143589-82-6

Basic information

• Product Name: Benzenemethanamine, 4-(1,1-dimethylethoxy)-.alpha.-methyl-
• Synonyms: Benzenemethanamine, 4-(1,1-dimethylethoxy)-.alpha.-methyl-;1-[4-[(2-methylpropan-2-yl)oxy]phenyl]ethanamine
• CAS NO: 143589-82-6
• Molecular Formula: C₁₂H₁₉NO
• Molecular Weight: 193.28536
• Mol File: 143589-82-6.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzenemethanamine, 4-(1,1-dimethylethoxy)-.alpha.-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanamine, 4-(1,1-dimethylethoxy)-.alpha.-methyl-(143589-82-6)
• EPA Substance Registry System: Benzenemethanamine, 4-(1,1-dimethylethoxy)-.alpha.-methyl-(143589-82-6)

Safety Data

• Hazardous Substances Data: 143589-82-6(Hazardous Substances Data)

Upstream product

• 4074-63-9 1-(4-(tert-butoxy)phenyl)ethan-1-one 
• 57699-45-3 p-tert-butoxybenzaldehyde 
• 75-16-1 methylmagnesium bromide 

Downstream Products

• 917911-58-1 N-[(R)-1-(4-tert-butoxyphenyl)ethyl]-2-methoxy-acetamide 
• 917911-59-2 (S)-1-(4-tert-butoxyphenyl)ethylamine sulfate 
• 143589-83-7 1-t-butyloxy-4-(1-amino-ethyl)-1,4-cyclohexadiene 

Relevant articles and documents

METHOD FOR PRODUCING OPTICALLY ACTIVE AMINOALKYLPHENOLS

The invention relates to a method for the enantioselective N-acylation of aminoalkylphenols, and to a method for producing enantiomer-pure compounds of formulae (I-S) and/or (I-R).

A novel constrained reduced-amide inhibitor of HIV-1 protease derived from the sequential incorporation of γ-turn mimetics into a model substrate

C7 mimetics, designed to lock three amino acid residues of a peptide chain into a γ-turn conformation, were introduced sequentially between the P3 to P2' positions of a model HIV-1 protease substrate I (resulting in compou