Category: 911052-85-2

Electric Literature of 911052-85-2, An article , which mentions 911052-85-2, molecular formula is C4H4BrNOS. The compound – (5-Bromothiazol-2-yl)methanol played an important role in people’s production and life.

The present invention provides novel phenicol derivatives, their use for the treatment of infections in mammals, pharmaceutical composition containing these novel compounds, and methods for the preparation of these compounds.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 911052-85-2, help many people in the next few years., Electric Literature of 911052-85-2

Reference：
Thiazole | C3H20NS – PubChem,
Thiazole | chemical compound | Britannica

911052-85-2, Name is (5-Bromothiazol-2-yl)methanol, molecular formula is C4H4BrNOS, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 911052-85-2, COA of Formula: C4H4BrNOS

Tosyl- and Boc-hydrazones were found to be effective nucleophiles in the Mitsunobu reaction. Tosyl hydrazones reacted cleanly with primary and secondary alcohols when co-administered to a cooled DBAD/PPh3 or DEAD/PPh 3 complex. Boc-hydrazones required electron-withdrawing substituents to participate in the reaction.

Tosyl- and Boc-hydrazones were found to be effective nucleophiles in the Mitsunobu reaction. Tosyl hydrazones reacted cleanly with primary and secondary alcohols when co-administered to a cooled DBAD/PPh3 or DEAD/PPh 3 complex. Boc-hydrazones required electron-withdrawing substituents to participate in the reaction.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.COA of Formula: C4H4BrNOS. In my other articles, you can also check out more blogs about 911052-85-2

Reference£º
Thiazole | C3H19NS – PubChem,
Thiazole | chemical compound | Britannica

911052-85-2, (5-Bromothiazol-2-yl)methanol is a thiazole compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

911052-85-2, (4-Bromo-thiazol-2-yl)-methanol (L. LG, 5.7 mmol) in DMF (15 ml) is treated at room temperature under nitrogen atmosphere with TRIFLUOROMETHANESULFONYL chloride (0.61 ml, 1 equivalent), and Et3N (0.8 ml, 1 equivalent). The reaction mixture is stirred for 3 hours at room temperature before the addition of sodium azide (1. 11 g, 3 equivalents), followed by overnight stirring at the same temperature. The reaction mixture is diluted with water and extracted with DCM and diethyl ether. The combined organic extracts are dried (MGSO4) and concentrated under reduced pressure to afford the crude product, which is used without purification in the next step.

The synthetic route of 911052-85-2 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; ARRAY BIOPHARMA, INC.; WO2004/46101; (2004); A2;,
Thiazole | C3H3NS – PubChem
Thiazole | chemical compound | Britannica