55915-75-8

Basic information

• Product Name: α-<((1,1-dimethylethyl)amino)methyl>-α-methylbenzenemethanol
• Synonyms: α-<((1,1-dimethylethyl)amino)methyl>-α-methylbenzenemethanol
• CAS NO: 55915-75-8
• Molecular Weight: 207.316
• Mol File: 55915-75-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: α-<((1,1-dimethylethyl)amino)methyl>-α-methylbenzenemethanol(CAS DataBase Reference)
• NIST Chemistry Reference: α-<((1,1-dimethylethyl)amino)methyl>-α-methylbenzenemethanol(55915-75-8)
• EPA Substance Registry System: α-<((1,1-dimethylethyl)amino)methyl>-α-methylbenzenemethanol(55915-75-8)

Safety Data

• Hazardous Substances Data: 55915-75-8(Hazardous Substances Data)

Upstream product

• 2085-88-3 2-methyl-2-phenyloxirane 
• 75-64-9 tert-butylamine 
• 85664-58-0 (Z)-2-methyl-N-(2-phenylpropylidene)propan-2-amine N-oxide 
• 34713-70-7 2-Phenylpropanal 
• 100812-08-6 2,2-Dimethyl-propionic acid 2-[(E)-tert-butylimino]-1-methyl-1-phenyl-ethyl ester 
• 50381-48-1 trioxo(N-tert-butylimido)osmium(VIII) 
• 98-83-9 isopropenylbenzene 

Relevant articles and documents

Bismuth (III) salts as catalysts in the opening of epoxides by amines

BiCl3 and Bi (OTf)3 catalyze the opening of epoxides (1-7) by amines (8-12). High regioselectivities are observed. BiCl3 et Bi (OTf)3 catalysent la reaction d'ouverture des epoxydes (1-7) par les amines (8-12). La reaction est fortement regioselective.

Preparation of Vicinal N-Alkylamino Alcohols via Acylation-Rearrangement of Nitrones Followed by Hydride Reduction

Acylation-rearrangement of N-tert-butyl and N-cyclohexyl nitrones of cyclohexanecarboxaldehyde (1), n-butyraldehyde, isobutyraldehyde, 3-cyclohexenecarboxaldehyde, and α-methylpropionaldehyde gave α-pivaloyloxy imines, which underwent reduction with lithi