Pang, Huan’s team published research in Chemical Communications (Cambridge, United Kingdom) in 2018 | CAS: 126456-43-7

(1S,2R)-1-Amino-2,3-dihydro-1H-inden-2-ol(cas: 126456-43-7) belongs to anime. Reduction of nitro compounds, RNO2, by hydrogen or other reducing agents produces primary amines cleanly (i.e., without a mixture of products), but the method is mostly used for aromatic amines because of the limited availability of aliphatic nitro compounds. Reduction of nitriles and oximes (R2C=NOH) also yields primary amines.Quality Control of (1S,2R)-1-Amino-2,3-dihydro-1H-inden-2-ol

In 2018,Chemical Communications (Cambridge, United Kingdom) included an article by Pang, Huan; Xu, Pingping; Li, Chonglu; Zhan, Yibei; Zhang, Zengyuan; Zhang, Wanshu; Yang, Guangfu; Sun, Yao; Li, Haibing. Quality Control of (1S,2R)-1-Amino-2,3-dihydro-1H-inden-2-ol. The article was titled 《A photo-responsive macroscopic switch constructed using a chiral azo-calix[4]arene functionalized silicon surface》. The information in the text is summarized as follows:

A photo-responsive macroscopic switch was fabricated using a chiral azo-calix[4]arene derivative (FC4AD) functionalized silicon surface and exhibited selective and reversible recognition of (1R,2S)-1-amino-2-indanol through the variation of wettability. This photo-responsive device may have wide applications in controlled release of chiral drugs and in biosensors. In the experimental materials used by the author, we found (1S,2R)-1-Amino-2,3-dihydro-1H-inden-2-ol(cas: 126456-43-7Quality Control of (1S,2R)-1-Amino-2,3-dihydro-1H-inden-2-ol)

(1S,2R)-1-Amino-2,3-dihydro-1H-inden-2-ol(cas: 126456-43-7) belongs to anime. Reduction of nitro compounds, RNO2, by hydrogen or other reducing agents produces primary amines cleanly (i.e., without a mixture of products), but the method is mostly used for aromatic amines because of the limited availability of aliphatic nitro compounds. Reduction of nitriles and oximes (R2C=NOH) also yields primary amines.Quality Control of (1S,2R)-1-Amino-2,3-dihydro-1H-inden-2-ol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Kong, Weifu’s team published research in Chemical Communications (Cambridge, United Kingdom) in 2019 | CAS: 34374-88-4

2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehyde(cas: 34374-88-4) is a member of phloroglucinol derivatives.Recommanded Product: 2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehydePhloroglucinols are known for their broad-spectrum antiviral, antibacterial, antifungal, antihelminthic, and phytotoxic activities.

In 2019,Chemical Communications (Cambridge, United Kingdom) included an article by Kong, Weifu; Jia, Wei; Wang, Rong; Gong, Yifan; Wang, Changchun; Wu, Peiyi; Guo, Jia. Recommanded Product: 2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehyde. The article was titled 《Amorphous-to-crystalline transformation toward controllable synthesis of fibrous covalent organic frameworks enabling promotion of proton transport》. The information in the text is summarized as follows:

Reversible imine exchange is adopted to molecularly re-arrange polyazomethine-based amorphous fibers into covalent organic frameworks (COFs) retaining pristine fibrous characters with periodic and oriented micropore channels. Such fibrous COFs can immobilize the assembled Nafion to form long-range proton conduction pathways, thus largely promoting proton transport. In addition to this study using 2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehyde, there are many other studies that have used 2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehyde(cas: 34374-88-4Recommanded Product: 2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehyde) was used in this study.

2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehyde(cas: 34374-88-4) is a member of phloroglucinol derivatives.Recommanded Product: 2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehydePhloroglucinols are known for their broad-spectrum antiviral, antibacterial, antifungal, antihelminthic, and phytotoxic activities.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Wang, Zhi-Qin’s team published research in Chemical Communications (Cambridge, United Kingdom) in 2019 | CAS: 821-41-0

5-Hexen-1-ol(cas: 821-41-0) is a volatile organic compound. Further, it is used to prepare 6-bromo-hex-1-ene by reaction with phosphorus tribromide.Electric Literature of C6H12O

In 2019,Chemical Communications (Cambridge, United Kingdom) included an article by Wang, Zhi-Qin; Tang, Xiao-Sheng; Yang, Zhao-Qi; Yu, Bao-Yi; Wang, Hua-Jing; Sang, Wei; Yuan, Ye; Chen, Cheng; Verpoort, Francis. Electric Literature of C6H12O. The article was titled 《Highly active bidentate N-heterocyclic carbene/ruthenium complexes performing dehydrogenative coupling of alcohols and hydroxides in open air》. The information in the text is summarized as follows:

Eight bidentate NHC/Ru complexes were designed and prepared In particular, compound I displayed extraordinary performance even in open air for the dehydrogenative coupling of alcs. and hydroxides. Notably, an unprecedentedly low catalyst loading of 250 ppm and the highest TON of 32 800 and TOF of 3200 until now were obtained. In the experimental materials used by the author, we found 5-Hexen-1-ol(cas: 821-41-0Electric Literature of C6H12O)

5-Hexen-1-ol(cas: 821-41-0) is a volatile organic compound. Further, it is used to prepare 6-bromo-hex-1-ene by reaction with phosphorus tribromide.Electric Literature of C6H12O

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Sasmal, Himadri Sekhar’s team published research in Journal of the American Chemical Society in 2019 | CAS: 34374-88-4

2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehyde(cas: 34374-88-4) is a member of phloroglucinol derivatives.Name: 2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehydeFor acyl phloroglucinols, it is considered the largest category of compounds among phloroglucinols of natural characteristics.

In 2019,Journal of the American Chemical Society included an article by Sasmal, Himadri Sekhar; Halder, Arjun; Kunjattu H, Shebeeb; Dey, Kaushik; Nadol, Athulya; Ajithkumar, Thalasseril G.; Ravindra Bedadur, Prachiti; Banerjee, Rahul. Name: 2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehyde. The article was titled 《Covalent Self-Assembly in Two Dimensions: Connecting Covalent Organic Framework Nanospheres into Crystalline and Porous Thin Films》. The information in the text is summarized as follows:

Insolubility of covalent organic frameworks (COFs) in organic solvents is one of the major obstacles for the potential application of these extended networks such as drug delivery, sensing, optoelectronics, and semiconductor device fabrication. The present work proposes a unique way to make uniform, solution-processable, crystalline, and porous COF nanospheres directly from the homogeneous solution of amine and aldehyde via spatial and temporal control of the nucleation and growth. This strategy of direct nucleation simultaneously showcases the caliber to tune the size of the COF nanospheres from 25 to 570 nm. We have also demonstrated the concept of mesoscale covalent self-assembly of those solution-processable COF nanospheres in the liquid-liquid interface (DCM-water bilayer) for the very first time, transmuting them into self-standing COF thin films with long-range ordered arrangements in two dimensions. The crystalline and porous (with TpAzo showing highest SBET of 1932 m2 g-1) free-standing COF thin films could be fabricated in a wide range of thicknesses from as low as 21 nm to as high as 630 nm. Both β-ketoenamine (TpAzo, TpDPP) and imine (TpOMeAzo, TpOMeDPP) linked COF thin films have been synthesized via mesoscale covalent self-assembly of the solution-processable COF nanospheres illustrating the generality of this eloquent methodol. Further, the solution processability has been tested and utilized to cast COF thin films uniformly in the inner and outer surface of an alumina hollow fiber membrane. The COF thin film-alumina hollow fiber membrane composites have showcased promising selective mol. separation of He and O2, He and CO2, and He and N2. The experimental process involved the reaction of 2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehyde(cas: 34374-88-4Name: 2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehyde)

2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehyde(cas: 34374-88-4) is a member of phloroglucinol derivatives.Name: 2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehydeFor acyl phloroglucinols, it is considered the largest category of compounds among phloroglucinols of natural characteristics.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Shirazi, Sanaz Gharehzadeh’s team published research in Journal of Chemical & Engineering Data in 2019 | CAS: 156-87-6

3-Aminopropan-1-ol(cas: 156-87-6) belongs to anime. Examples of direct uses of amines and their salts are as corrosion inhibitors in boilers and in lubricating oils (morpholine), as antioxidants for rubber and roofing asphalt (diarylamines), as stabilizers for cellulose nitrate explosives (diphenylamine), as protectants against damage from gamma radiation (diarylamines), as developers in photography (aromatic diamines), as flotation agents in mining, as anticling and waterproofing agents for textiles, as fabric softeners, in paper coating, and for solubilizing herbicides.Name: 3-Aminopropan-1-ol

In 2019,Journal of Chemical & Engineering Data included an article by Shirazi, Sanaz Gharehzadeh; Kermanpour, Fakhri. Name: 3-Aminopropan-1-ol. The article was titled 《Density and Viscosity of 2-Butanol + (1-Propanol, 2-Propanol, or 3-Amino-1-propanol) Mixtures at Temperatures of (293.15 to 323.15) K: Application of the ERAS Model》. The information in the text is summarized as follows:

D., ρ, and viscosity, η, of pure components 1-propanol, 2-propanol, 3-amino-1-propanol, and 2-butanol along with binary mixtures of {x12-butanol + x21-propanol}, {x12-butanol + x22-propanol}, and {x12-butanol + x23-amino-1-propanol} were determined over the entire composition range at temperatures of (293.15 to 323.15) K. The exptl. data of d. and viscosity were used to calculate the excess molar volumes, VmE, and viscosity deviations, Δη, of the mixtures The obtained results show that the VmE values of the mixtures are neg. over the whole composition range and increase with increasing temperature Viscosity deviations of the {x12-butanol + x21-propanol} mixture are neg. at low temperatures and pos. at high temperatures, while the Δη values of {x12-butanol + x22-propanol} and {x12-butanol + x23-amino-1-propanol} mixtures are neg. over the whole composition range and decrease with increasing temperature The excess molar quantities were correlated by the Redlich-Kister equation. The ERAS model was used to correlate the excess molar volumes of the mixtures at temperatures of (298.15, 303.15, 313.15) K. Comparison between the calculated and exptl. VmE values shows good agreement for all three mixtures The results came from multiple reactions, including the reaction of 3-Aminopropan-1-ol(cas: 156-87-6Name: 3-Aminopropan-1-ol)

3-Aminopropan-1-ol(cas: 156-87-6) belongs to anime. Examples of direct uses of amines and their salts are as corrosion inhibitors in boilers and in lubricating oils (morpholine), as antioxidants for rubber and roofing asphalt (diarylamines), as stabilizers for cellulose nitrate explosives (diphenylamine), as protectants against damage from gamma radiation (diarylamines), as developers in photography (aromatic diamines), as flotation agents in mining, as anticling and waterproofing agents for textiles, as fabric softeners, in paper coating, and for solubilizing herbicides.Name: 3-Aminopropan-1-ol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Luo, Maolan’s team published research in Chemical Communications (Cambridge, United Kingdom) in 2019 | CAS: 34374-88-4

2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehyde(cas: 34374-88-4) is a member of phloroglucinol derivatives. Regarding monomeric phloroglucinols, this group encompasses acryl phloroglucinols, phloroglucinol-terpene adducts, phloroglucinol glycosides, halogenated phloroglucinols, prenylated phloroglucinols, and cyclicroup polyketides.Electric Literature of C9H6O6

The author of 《Boosting photocatalytic H2 evolution on g-C3N4 by modifying covalent organic frameworks (COFs)》 were Luo, Maolan; Yang, Qing; Liu, Kewei; Cao, Hongmei; Yan, Hongjian. And the article was published in Chemical Communications (Cambridge, United Kingdom) in 2019. Electric Literature of C9H6O6 The author mentioned the following in the article:

Modifying g-C3N4 with covalent organic frameworks (COFs) through imine linkage results in a dramatically enhanced visible-light-driven photocatalytic hydrogen evolution, which reached 10.1 mmol g-1 h-1 when 2 wt% Pt and triethanolamine were used as co-catalyst and sacrificial agent, resp., corresponding to an apparent quantum efficiency (AQE) of 20.7% at 425 nm. The experimental process involved the reaction of 2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehyde(cas: 34374-88-4Electric Literature of C9H6O6)

2,4,6-Trihydroxybenzene-1,3,5-tricarbaldehyde(cas: 34374-88-4) is a member of phloroglucinol derivatives. Regarding monomeric phloroglucinols, this group encompasses acryl phloroglucinols, phloroglucinol-terpene adducts, phloroglucinol glycosides, halogenated phloroglucinols, prenylated phloroglucinols, and cyclicroup polyketides.Electric Literature of C9H6O6

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Cui, Yunshu’s team published research in Chemical Communications (Cambridge, United Kingdom) in 2020 | CAS: 24388-23-6

4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane(cas: 24388-23-6) can be used as a substrate in the study of Suzuki–Miyaura coupling of various aryl iodides over SiliaCat Pd(0).Application In Synthesis of 4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane

《Storage and release of two electrons from an electron-rich carbon-carbon bond: boron mediated reversible coupling of DMAP and 9-azajulolidine》 was published in Chemical Communications (Cambridge, United Kingdom) in 2020. These research results belong to Cui, Yunshu; Xiang, Libo; Wang, Junyi; Li, Chunlei; Hao, Wei; Ye, Qing. Application In Synthesis of 4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane The article mentions the following:

This manuscript describes the preparation of [{(dpp-bian)BBr}Li(DME)3] (2, dpp-bian = 1,2-bis[(2,6-diisopropylphenyl) imino]acenaphthene) and [{(dpp-bian)BL}+Br-] (5, L = DMAP; 6, L = 9-azajulolidine). The 4,4-coupling of DMAP and 2,2-coupling of 9-azajulolidine can be achieved either by the reaction of 2 with L, or by one-electron reduction of borenium cations 5 and 6. Oxidation of 3 and 4 leads to C-C cleavage and regeneration of 5 and 6. All new compounds were structurally characterized. In the experiment, the researchers used many compounds, for example, 4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane(cas: 24388-23-6Application In Synthesis of 4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane)

4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane(cas: 24388-23-6) can be used as a substrate in the study of Suzuki–Miyaura coupling of various aryl iodides over SiliaCat Pd(0).Application In Synthesis of 4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Iacopetta, Domenico’s team published research in International Journal of Molecular Sciences in 2020 | CAS: 26153-38-8

3,5-Dihydroxybenzaldehyde(cas: 26153-38-8) is used as a building block in the synthesis of more complex structures. It is also used in the synthesis of terbutaline, which is an important bronchodilator.Name: 3,5-Dihydroxybenzaldehyde

《Newly synthesized imino-derivatives analogues of resveratrol exert inhibitory effects in breast tumor cells》 was published in International Journal of Molecular Sciences in 2020. These research results belong to Iacopetta, Domenico; Lappano, Rosamaria; Mariconda, Annaluisa; Ceramella, Jessica; Sinicropi, Maria Stefania; Saturnino, Carmela; Talia, Marianna; Cirillo, Francesca; Martinelli, Fabio; Puoci, Francesco; Rosano, Camillo; Longo, Pasquale; Maggiolini, Marcello. Name: 3,5-Dihydroxybenzaldehyde The article mentions the following:

Breast cancer represents the most frequently diagnosed malignancy in women worldwide. Various therapeutics are currently used in order to halt the progression of breast tumor, even though certain side effects may limit the beneficial effects. In recent years, many efforts have been addressed to the usefulness of natural compounds as anticancer agents due to their low toxicity. Resveratrol, a stilbene found in grapes, berries, peanuts and soybeans, has raised a notable interest for its antioxidant, anti-inflammatory, and antitumor properties. Here, we report the design, the synthesis and the characterization of the anticancer activity of a small series of imino N-aryl-substituted compounds that are analogs of resveratrol. In particular, the most active compound, named 3, exhibited anti-tumor activity in diverse types of breast cancer cells through the inhibition of the human topoisomerase II and the induction of apoptotic cell death. Therefore, the abovementioned compound maybe considered as a promising agent in more comprehensive treatments of breast cancer.3,5-Dihydroxybenzaldehyde(cas: 26153-38-8Name: 3,5-Dihydroxybenzaldehyde) was used in this study.

3,5-Dihydroxybenzaldehyde(cas: 26153-38-8) is used as a building block in the synthesis of more complex structures. It is also used in the synthesis of terbutaline, which is an important bronchodilator.Name: 3,5-Dihydroxybenzaldehyde

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Requejo, Patricia F.’s team published research in Industrial & Engineering Chemistry Research in 2020 | CAS: 6381-59-5

Potassium sodium (2R,3R)-2,3-dihydroxysuccinate tetrahydrate(cas: 6381-59-5) is a ferroelectric crystal with a high piezoelectric effect and electromechanical coupling coefficient. Application of 6381-59-5 Potassium sodium tartrate tetrahydrate has been used in the preparation of Lowry reagent for the determination of microsomal protein concentration in rat hepatic microsomes by Lowry method.

《Study of Liquid-Liquid Equilibrium of Aqueous Two-Phase Systems Based on Ethyl Lactate and Partitioning of Rutin and Quercetin》 was written by Requejo, Patricia F.; Velho, Pedro; Gomez, Elena; Macedo, Eugenia A.. Application of 6381-59-5 And the article was included in Industrial & Engineering Chemistry Research in 2020. The article conveys some information:

Two Et lactate (EL)-based aqueous two-phase systems (ATPSs) were studied at T = 298.15 K and atm. pressure. Sodium tartrate and potassium sodium tartrate organic salts have been used to form biphasic systems. To assess the phase splitting, binodal curves and tie-lines were obtained exptl. by the cloud point method and a technique, which consist of the d. and refractive index, resp. Binodal curves were fitted with the Merchuk equation obtaining a good fit. Moreover, modeling with the universal quasichem. thermodn. equation was carried out to accurately represent the two-biphasic systems. Furthermore, exptl. binodal curves obtained in this work and literature results for the same systems and for systems with EL and other salts were analyzed regarding their similarity. Finally, the application of the adopted ATPS in the partitioning of two flavonoids, rutin and quercetin, was studied in terms of the partition coefficients and the percentage of extraction Rutin and quercetin showed better affinity to the EL-rich phase, evidencing that the use of the proposed ATPS may be a successful technique in the biotechnol. industry for the separation of each flavonoid. In the experiment, the researchers used many compounds, for example, Potassium sodium (2R,3R)-2,3-dihydroxysuccinate tetrahydrate(cas: 6381-59-5Application of 6381-59-5)

Potassium sodium (2R,3R)-2,3-dihydroxysuccinate tetrahydrate(cas: 6381-59-5) is a ferroelectric crystal with a high piezoelectric effect and electromechanical coupling coefficient. Application of 6381-59-5 Potassium sodium tartrate tetrahydrate has been used in the preparation of Lowry reagent for the determination of microsomal protein concentration in rat hepatic microsomes by Lowry method.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Wang, Lucia’s team published research in Chemical Communications (Cambridge, United Kingdom) in 2021 | CAS: 78782-17-9

Bis[(pinacolato)boryl]methane(cas: 78782-17-9) belongs to organoboron compounds. Organoboron compounds have been a cornerstone of synthetic transformations for decades. Areas such as boron-containing catalysts, metalate chemistry, photoredox methods, and boryl anions have brought significant new developments in understanding and provided new reactivity upon.Electric Literature of C13H26B2O4

Wang, Lucia; Lin, Shengjia; Zhu, Yawei; Ferrante, Daniel; Ishak, Timaf; Baba, Yuki; Sharma, Abhishek published their research in Chemical Communications (Cambridge, United Kingdom) in 2021. The article was titled 《α-Hydroxy boron-enabled regioselective access to bifunctional halo-boryl alicyclic ethers and α-halo borons》.Electric Literature of C13H26B2O4 The article contains the following contents:

α-Hydroxy borons are an underused class of compounds and their only previous application involved oxidation into acylborons. Herein, the authors describe the synthesis of functionalized olefinic α-hydroxy borons and their utility to enable a novel and regioselective route to hitherto unknown bifunctional halo-boryl tetrahydrofurans/tetrahydropyrans and α-halo MIDA boronates. The orthogonally functionalized alicyclic ethers provided a building block-based approach for diversification of the THF core. In the experimental materials used by the author, we found Bis[(pinacolato)boryl]methane(cas: 78782-17-9Electric Literature of C13H26B2O4)

Bis[(pinacolato)boryl]methane(cas: 78782-17-9) belongs to organoboron compounds. Organoboron compounds have been a cornerstone of synthetic transformations for decades. Areas such as boron-containing catalysts, metalate chemistry, photoredox methods, and boryl anions have brought significant new developments in understanding and provided new reactivity upon.Electric Literature of C13H26B2O4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts