62965-15-5

Basic information

• Product Name: L-Alanine, 3-bromo-N-[(phenylmethoxy)carbonyl]-, methyl ester
• CAS NO: 62965-15-5
• Molecular Formula: C12H14BrNO4
• Molecular Weight: 316.151
• Mol File: 62965-15-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: L-Alanine, 3-bromo-N-[(phenylmethoxy)carbonyl]-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: L-Alanine, 3-bromo-N-[(phenylmethoxy)carbonyl]-, methyl ester(62965-15-5)
• EPA Substance Registry System: L-Alanine, 3-bromo-N-[(phenylmethoxy)carbonyl]-, methyl ester(62965-15-5)

Safety Data

• Hazardous Substances Data: 62965-15-5(Hazardous Substances Data)

Upstream product

• 1492-52-0 methyl (S)-2-(benzyloxycarbonlamino)-3-(p-toluenesulfonyl)propionate 
• 1145-80-8 N-(benzyloxycarbonyl)-L-serine 
• 1676-81-9 N-benzyloxycarbonyl-L-serine methyl ester 

Downstream Products

• 56877-40-8 Z-γ,γ,-di-tert-butyl-D,L-carboxyglutamic acid methyl ester 
• 3693-95-6 N,N'-bis[(phenylmethoxy)carbonyl]-L-cystine 1,1'-dimethyl ester 
• 56877-43-1 Z-DL-Gla(OtBu)2-OH 
• 200344-43-0 methyl R(S)-3-diphenylphosphanylmethyl-N-carbobenzyloxyserinate 
• 200344-44-1 methyl R(S)-3-diphenylarsanylmethyl-N-carbobenzyloxyserinate 

Relevant articles and documents

Magnetic-field-dependent 1H relaxivity behavior of biotin/avidin-based magnetic resonance imaging probes

One major challenge in noninvasive mapping of various molecular targets is their inherently low in vivo concentration coupled with the insensitivity of imaging modalities, such as the widely used magnetic resonance imaging (MRI). Development of agents wit

Visible-light-mediated conversion of alcohols to halides

The development of new means of activating molecules and bonds for chemical reactions is a fundamental objective for chemists. In this regard, visible-light photoredox catalysis has emerged as a powerful technique for chemoselective activation of chemical bonds under mild reaction conditions. Here, we report a visible-light-mediated photocatalytic alcohol activation, which we use to convert alcohols to the corresponding bromides and iodides in good yields, with exceptional functional group tolerance. In this fundamentally useful reaction, the design and operation of the process is simple, the reaction is highly efficient, and the formation of stoichiometric waste products is minimized.

One pot conversion of alcohols to disulfides mediated by benzyltriethylammonium tetrathiomolybdate

A one pot conversion of alcohols to disulfides in good yields via the activation of a hydroxyl group with DCC or P(NMe2)3 / CCl4 followed by treatment with benzyltriethylammonium tetrathiomolybdate is reported.