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《Effect of the fluorination degree of partially fluorinated octyl-phosphocholine surfactants on their interfacial properties and interactions with purple membrane as a membrane protein model》 was written by Baba, Teruhiko; Takagi, Toshiyuki; Sumaru, Kimio; Kanamori, Toshiyuki. Category: alcohols-buliding-blocks And the article was included in Chemistry and Physics of Lipids in 2020. The article conveys some information:

Interfacial properties and membrane protein solubilization activity of a series of partially fluorinated octyl-phosphocholine (PC) surfactants were investigated from the viewpoint of the fluorination degree of the hydrophobic chain. The critical micelle concentration (CMC), surface tension lowering activity, mol. occupied area at the CMC and free energy changes of micellization as well as adsorption to the air-water interface for each PC surfactant were estimated from surface tension measurements at 25 °C. The PCs with higher degree of fluorination exhibited low CMC and high surface activity, while the single trifluoromethyl group at the end of the chain appeared to enhance the hydrophilicity of the surfactant mol. Under conditions where conventional short-chain surfactants, n-octyl-β-D-glucoside, Triton X-100 and dioctanoylphosphatidylcholine significantly solubilize purple membranes (PM), none of the fluorinated-PCs solubilized PM. This suggests that fluorinated-PCs are low-invasive enough to maintain the structure of lipids/protein assemblies like PM. After reading the article, we found that the author used 5-Hexen-1-ol(cas: 821-41-0Category: alcohols-buliding-blocks)

5-Hexen-1-ol(cas: 821-41-0) is used in cyclization to a tetrahydropyran by phenylselenoetherification. It is also used as a building block in synthetic chemistry.Category: alcohols-buliding-blocks

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

The author of 《Use of Nitrogen-Doped Carbon Nanodots for the Photocatalytic Fluoroalkylation of Organic Compounds》 were Rosso, Cristian; Filippini, Giacomo; Prato, Maurizio. And the article was published in Chemistry – A European Journal in 2019. Product Details of 821-41-0 The author mentioned the following in the article:

The use of amine-rich N-doped carbon nanodots (NCNDs) for the photochem. radical perfluoroalkylation of organic compounds e.g., mesitylene is reported. This operationally simple approach occurs under mild conditions producing valuable new C-C bonds e.g., 1,3,5-trimethyl-2-(perfluorohexyl)benzene. The chem. is driven by the ability of NCNDs to directly reach an electronically excited state upon light absorption, thereby successively triggering the formation of reactive radical species from simple perfluoroalkyl iodides RI [R = C6F13, C4F9, C8F17, CF(CF3)2]. Preliminary mechanistic studies are also reported. The experimental process involved the reaction of 5-Hexen-1-ol(cas: 821-41-0Product Details of 821-41-0)

5-Hexen-1-ol(cas: 821-41-0) is used in cyclization to a tetrahydropyran by phenylselenoetherification. It is also used as a building block in synthetic chemistry.Product Details of 821-41-0

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

In 2019,Reactive & Functional Polymers included an article by Bialek, Marzena; Fryga, Julia. Category: alcohols-buliding-blocks. The article was titled 《Effective copolymerization of ethylene with α,ω-alkenols and homopolymerization of α,ω-alkenols catalyzed by aminophenolate zirconium complex》. The information in the text is summarized as follows:

A zirconium complex of diamine-bis(phenolate) ligand, [(tBu2O2NN’)ZrCl]2(μ-O) where (tBu2O2NN’) = Me2N(CH2)2N(CH2-2-O–3,5-tBu2-C6H2)2, activated with (iBu)3Al/Ph3CB(C6F5)4, was for the first time used in copolymerization of ethylene with unsaturated alcs. (CH2 = CH(CH2)nCH2OH, where n = 7, 8, 3). The hydroxyl groups of comonomers were protected with R3-xAlClx (where x = 0 or 1, R = iBu, Et). In contrast to the formerly reported catalysts, the activity of this catalyst is much higher in ethylene/alkenols copolymerization than in ethylene homopolymerization and its lifetime is long. Moreover, the copolymers with high polar comonomer contents (up to 16.4 mol%, 52.3 wt%) were produced. The effects of copolymerization conditions such as comonomer/protecting agent molar ratio, comonomer concentration, ethylene pressure and reaction time on the catalyst activity and comonomer incorporation were studied. In addition, polyalkenols were synthesized by the coordination polymerization of α,ω-alkenols with the use of [(tBu2O2NN’)ZrCl]2(μ-O) and rac-Et(Ind)2ZrCl2 for reference DSC, TG, GPC, SEM, 1H and 13C NMR, and FTIR methods were used to characterize the (co)polymerization products. In the experimental materials used by the author, we found 5-Hexen-1-ol(cas: 821-41-0Category: alcohols-buliding-blocks)

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.Category: alcohols-buliding-blocks

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Poggini, Lorenzo; Tancini, Erik; Danieli, Chiara; Sorrentino, Andrea Luigi; Serrano, Giulia; Lunghi, Alessandro; Malavolti, Luigi; Cucinotta, Giuseppe; Barra, Anne-Laure; Juhin, Amelie; Arrio, Marie-Anne; Li, Weibin; Otero, Edwige; Ohresser, Philippe; Joly, Loic; Kappler, Jean Paul; Totti, Federico; Sainctavit, Philippe; Caneschi, Andrea; Sessoli, Roberta; Cornia, Andrea; Mannini, Matteo published an article in 2021. The article was titled 《Engineering Chemisorption of Fe4 Single-Molecule Magnets on Gold》, and you may find the article in Advanced Materials Interfaces.Recommanded Product: 821-41-0 The information in the text is summarized as follows:

Gaining control over the grafting geometry is critically important for any application of surface-supported single-mol. magnets (SMMs) in data storage, spintronics, and quantum information science. Here, tetrairon(III) SMMs with a propeller-like structure are functionalized with thioacetyl-terminated alkyl chains to promote chemisorption on gold surfaces from solution and to evaluate differences in adsorption geometry and magnetic properties as a function of chain length. The prepared monolayers are investigated using X-ray absorption techniques with linearly and circularly polarized light to extract geometrical and magnetic information, resp. All derivatives remain intact and form partially oriented monolayers on the gold surface. A ligand-field anal. of the observed X-ray natural linear dichroism shows that the threefold mol. axis is invariably biased toward the surface normal, in agreement with ab initio calculations This preferential orientation is most pronounced in monolayers of the shortest-chain derivative, which are further studied with an ultralow temperature X-ray magnetic CD setup operating down to 350 mK. The isothermal field sweeps with the magnetic field at normal incidence show an open hysteresis loop below 1 K, while measurements at different incidence angles prove the magnetic anisotropy of the monolayers. After reading the article, we found that the author used 5-Hexen-1-ol(cas: 821-41-0Recommanded Product: 821-41-0)

5-Hexen-1-ol(cas: 821-41-0) is used in cyclization to a tetrahydropyran by phenylselenoetherification. It is also used as a building block in synthetic chemistry.Recommanded Product: 821-41-0

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

In 2019,Advanced Functional Materials included an article by Kubiak, Joshua M.; MacFarlane, Robert J.. SDS of cas: 821-41-0. The article was titled 《Forming Covalent Crosslinks between Polymer-Grafted Nanoparticles as a Route to Highly Filled and Mechanically Robust Nanocomposites》. The information in the text is summarized as follows:

Filler aggregation in polymer matrix nanocomposites leads to inhomogeneity in particle distribution and deterioration of mech. properties. The use of polymer-grafted nanoparticles (PGNPs) with polymers directly attached to the particle surfaces precludes aggregation of the filler. However, solids composed of PGNPs are mech. weak unless the grafted chains are long enough to form entanglements between particles, and requiring long grafts limits the achievable filler d. of the nanocomposite. In this work, long, entangled grafts are replaced with short reactive polymers that form covalent crosslinks between particles. Crosslinkable PGNPs, referred to as XNPs, can be easily processed from solution and subsequently cured to yield a highly filled yet mech. robust composite. In this specific instance, silica nanoparticles are grafted with poly(glycidyl methacrylate), cast into films, and crosslinked with multifunctional amines at elevated temperatures Indentation and scratch experiments show significant enhancement of hardness, modulus, and scratch resistance compared to non-crosslinked PGNPs and to crosslinked polymer films without nanoparticle reinforcement. Loadings of up to 57 wt% are achieved while yielding uniform films that deform locally in a predominantly elastic manner. XNPs therefore potentially allow for the formulation of robust nanocomposites with a high level of functionality imparted by the selected filler particles. In addition to this study using 5-Hexen-1-ol, there are many other studies that have used 5-Hexen-1-ol(cas: 821-41-0SDS of cas: 821-41-0) was used in this study.

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.SDS of cas: 821-41-0

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Formula: C6H12OIn 2019 ,《Systematically Controlled Decomposition Mechanism in Phosphorus Flame Retardants by Precise Molecular Architecture: P-O vs P-N》 was published in ACS Applied Polymer Materials. The article was written by Markwart, Jens C.; Battig, Alexander; Zimmermann, Lisa; Wagner, Martin; Fischer, Jochen; Schartel, Bernhard; Wurm, Frederik R.. The article contains the following contents:

Flame retardants (FR) are inevitable additives to many plastics. Halogenated organics are effective FRs but are controversially discussed due to the release of toxic gases during a fire or their persistence if landfilled. Phosphorus-containing compounds are effective alternatives to halogenated FRs and have potential lower toxicity and degradability. In addition, nitrogen-containing additives were reported to induce synergistic effects with phosphorus-based FRs. However, no systematic study of the gradual variation on a single phosphorus FR containing both P-O and P-N moieties and their comparison to the resp. blends of phosphates and phosphoramides was reported. This study developed general design principles for P-O- and P-N-based FRs and will help to design effective FRs for various polymers. We synthesized a library of phosphorus FRs that only differ in their P-binding pattern from each other and studied their decomposition mechanism in epoxy resins. Systematic control over the decomposition pathways of phosphate (P=O(OR)3), phosphoramidate (P=O(OR)2(NHR)), phosphorodiamidate (P=O(OR)(NHR)2), phosphoramide (P=O(NHR)3), and their blends was identified, for example, by reducing cis-elimination and the formation of P-N-rich char with increasing nitrogen content in the P-binding sphere. Our FR epoxy resins can compete with com. FRs in most cases, but we proved that the blending of esters and amides outperformed the single-mol. amidates/diamidates due to distinctively different decomposition mechanisms acting synergistically when blended. The results came from multiple reactions, including the reaction of 5-Hexen-1-ol(cas: 821-41-0Formula: C6H12O)

5-Hexen-1-ol(cas: 821-41-0) is used in cyclization to a tetrahydropyran by phenylselenoetherification. It is also used as a building block in synthetic chemistry.Formula: C6H12O

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Product Details of 821-41-0In 2020 ,《Rhodium-Catalyzed Remote C(sp3)-H Borylation of Silyl Enol Ethers》 appeared in Angewandte Chemie, International Edition. The author of the article were Li, Jie; Qu, Shuanglin; Zhao, Wanxiang. The article conveys some information:

A rhodium-catalyzed remote C(sp3)-H borylation of silyl enol ethers (SEEs, E/Z mixtures) by alkene isomerization and hydroboration is reported. The reaction exhibits mild reaction conditions and excellent functional-group tolerance. This method is compatible with an array of SEEs, including linear and branched SEEs derived from aldehydes and ketones, and provides direct access to a broad range of structurally diverse 1,n-borylethers in excellent regioselectivities and good yields. These compounds are precursors to various valuable chems., such as 1,n-diols and amino alcs. The results came from multiple reactions, including the reaction of 5-Hexen-1-ol(cas: 821-41-0Product Details of 821-41-0)

5-Hexen-1-ol(cas: 821-41-0) is used in cyclization to a tetrahydropyran by phenylselenoetherification. It is also used as a building block in synthetic chemistry.Product Details of 821-41-0

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

In 2022,Blair, Daniel J.; Chitti, Sriyankari; Trobe, Melanie; Kostyra, David M.; Haley, Hannah M. S.; Hansen, Richard L.; Ballmer, Steve G.; Woods, Toby J.; Wang, Wesley; Mubayi, Vikram; Schmidt, Michael J.; Pipal, Robert W.; Morehouse, Greg. F.; Palazzolo Ray, Andrea M. E.; Gray, Danielle L.; Gill, Adrian L.; Burke, Martin D. published an article in Nature (London, United Kingdom). The title of the article was 《Automated iterative Csp3-C bond formation》.Product Details of 821-41-0 The author mentioned the following in the article:

Fully automated synthetic chem. would substantially change the field by providing broad on-demand access to small mols. However, the reactions that can be run autonomously are still limited. Automating the stereospecific assembly of Csp3-C bonds would expand access to many important types of functional organic mols.1. Previously, methyliminodiacetic acid (MIDA) boronates were used to orchestrate the formation of Csp2-Csp2 bonds and were effective building blocks for automating the synthesis of many small mols., but they are incompatible with stereospecific Csp3-Csp2 and Csp3-Csp3 bond-forming reactions. Here authors report that hyperconjugative and steric tuning provide a new class of tetra-Me N-methyliminodiacetic acid (TIDA) boronates that are stable to these conditions. Charge d. anal. revealed that redistribution of electron d. increases covalency of the N-B bond and thereby attenuates its hydrolysis. Complementary steric shielding of carbonyl π-faces decreases reactivity towards nucleophilic reagents. The unique features of the iminodiacetic acid cage, which are essential for generalized automated synthesis, are retained by TIDA boronates. This enabled Csp3 boronate building blocks to be assembled using automated synthesis, including the preparation of natural products through automated stereospecific Csp3-Csp2 and Csp3-Csp3 bond formation. These findings will enable increasingly complex Csp3-rich small mols. to be accessed via automated assembly. In the experiment, the researchers used many compounds, for example, 5-Hexen-1-ol(cas: 821-41-0Product Details of 821-41-0)

5-Hexen-1-ol(cas: 821-41-0) is used in cyclization to a tetrahydropyran by phenylselenoetherification. It is also used as a building block in synthetic chemistry.Product Details of 821-41-0

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

The author of 《Mediator and Additive Free Trifluoromethyl-Fluorination of Terminal Alkenes by Persistent Perfluoroalkyl Radical》 were Sato, Azusa; Ponomarenko, Maksym V.; Ono, Taizo; Roeschenthaler, Gerd-Volker; Soloshonok, Vadim A.. And the article was published in European Journal of Organic Chemistry in 2019. Related Products of 821-41-0 The author mentioned the following in the article:

It was found that the persistent perfluoro-3-ethyl-2,4-dimethyl-3-pentyl radical (PPFR) could serve as a source of both trifluoromethyl-radical and fluorine atom in the reactions with terminal olefins. The dual reactivity of the persistent PPFR allowed for both trifluoromethylation and fluorination of terminal olefins. This new approach towards di-functionalized 1-CF3-2-F-alkanes RCHFCH2CF3 [R = CH2HC(CO2Et)2, Bn, 3-ClC6H4CH2, etc.] demonstrated the widespread synthetic potential. Preliminary data strongly suggested potentially high synthetic value of this methodol. new transformation. The results came from multiple reactions, including the reaction of 5-Hexen-1-ol(cas: 821-41-0Related Products of 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.Related Products of 821-41-0

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Lenormand, Anthony; Reyes Mendez, Lucia; Coulomb, Julien published their research in Chemistry – A European Journal in 2021. The article was titled 《Relay-Heck Cross-Coupling Between Alkenyl Halides and Unsaturated Alcohols in the Synthesis of Open-Chain Analogues of Musk Odorant Vulcanolide》.Related Products of 821-41-0 The article contains the following contents:

Unactivated alkenyl iodides and bromides underwent an unprecedented palladium-catalyzed relay-Heck cross-coupling with a whole range of alkenols of different chain lengths linking the alkene and the alc., affording unsaturated aldehydes and ketones in moderate to good yields. In contrast, alkenyl triflates were not suitable partners for this reaction. This method allowed the preparation of open-chain analogs of the musk odorant Vulcanolide, several of which retained key olfactory properties of the parent mol. The experimental process involved the reaction of 5-Hexen-1-ol(cas: 821-41-0Related Products of 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.Related Products of 821-41-0

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts