New learning discoveries about 1072-52-2

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles. 1072-52-2, 2-(Aziridin-1-yl)ethanol, other downstream synthetic routes, hurry up and to see.

Application of 1072-52-2, Adding some certain compound to certain chemical reactions, such as: 1072-52-2, name is 2-(Aziridin-1-yl)ethanol,molecular formula is C4H9NO, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 1072-52-2.

EXAMPLE 9 4-(2-hydroxyethyl)-3-thiamorpholinone (Compound 14) To a solution, stirred at ambient temperature, of 120 g of ethyl thioglycolate (1 mole) in 300 cm3 of absolute ethanol, placed under an inert atmosphere, there is slowly added a solution of 87 g (1 mole) of N-(2-hydroxyethyl)aziridine diluted in 100 cm3 of ethanol. The reaction is exothermic and the temperature of the reaction mixture is maintained at a temperature lower than 50 C. One half hour after the end of the introduction, the solution is brought to reflux for 6 hours. The ethanol is then removed and the resulting liquid is distilled under reduced pressure. BP/0.1-0.3 mm=167-170 C. The 4-(2-hydroxyethyl)-3-thiamorpholinone is a light yellow, viscous and hygroscopic liquid whose elemental analysis under the hydrated form is as follows:

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles. 1072-52-2, 2-(Aziridin-1-yl)ethanol, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; L’Oreal; US4539320; (1985); A;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

New downstream synthetic route of 1072-52-2

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,1072-52-2, its application will become more common.

Adding a certain compound to certain chemical reactions, such as: 1072-52-2, 2-(Aziridin-1-yl)ethanol, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound, 1072-52-2, blongs to alcohols-buliding-blocks compound. Computed Properties of C4H9NO

Example 20 (Scheme 15): Preparation of 2-((2-bromoethyl)-2-{ll-[2-((2-bromoethyl){2- [(methylsulfonyl)oxy] ethyl} amino)-3,5-dinitrophenyl] -6-hydroxy-6-oxido-ll-oxo-5,7- dioxa-2,10-diaza-6-phosphaundec-l-anoyl}-4,6-dinitroanilino)ethyl methanesulfonate(52); Reaction of 37 as in Scheme 15 gave 2-((2-bromoethyl)-2-{l l-[2-((2-bromoethyl){2- [(methylsulfonyl)oxy]ediyl}arnino)-3,5-dinitrophenyl]-6-oxido-ll-oxo-5,7-dioxa-2,10-diaza-6- phosphaundec-l-anoyl}-4,6-dinitroanilino)ethyl methanesulfonate (51) as a yellow oil: 1H NMR [(CDj)2SO] delta 8.99 (t, / = 5.6 Hz, 2 H), 8.75 (d, / = 2.8 Hz, 2 H), 8.40 (d, / = 2.8 Hz, 2 H), 6.98 (dj = 709 Hz, 1 H), 4.28 (t,/ = 5.5 Hz, 4 H), 4.20 (m, 4 H), 3.58 (m, 8 H), 3.48 (m, 8 H), 3.13 (s, 6 H); 13C NMR delta 165.5, 145.9, 145.3, 140.9, 135.6, 127.6, 122.4, 67.4, 63.4, 54.3, 51.1, 39.7, 36.4, 29.7; HRMS (FAB) calcd for C28H3879Br2N8O19PS2 [M+H]+ m/Z 1042.9799; found 1042.9786.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,1072-52-2, its application will become more common.

Reference:
Patent; AUCKLAND UNISERVICES LIMITED; WO2008/30112; (2008); A1;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts