676457-76-4

Basic information

• Product Name: Carbamic acid, [(1S)-1-(bromomethyl)-2-phenylethyl]-, phenylmethyl ester
• CAS NO: 676457-76-4
• Molecular Formula: C17H18BrNO2
• Molecular Weight: 348.239
• Mol File: 676457-76-4.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Carbamic acid, [(1S)-1-(bromomethyl)-2-phenylethyl]-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [(1S)-1-(bromomethyl)-2-phenylethyl]-, phenylmethyl ester(676457-76-4)
• EPA Substance Registry System: Carbamic acid, [(1S)-1-(bromomethyl)-2-phenylethyl]-, phenylmethyl ester(676457-76-4)

Safety Data

• Hazardous Substances Data: 676457-76-4(Hazardous Substances Data)

Upstream product

• 3397-32-8 N-(benzyloxycarbonyl)-phenylalanine-N-hydroxysuccinimide ester 
• 6372-14-1 N-((benzyloxy)carbonyl)-L-phenylalaninol 

Downstream Products

• 1334324-91-2 C₂₀H₂₃NO₂S 
• 1334324-83-2 (S,E)-benzyl (1-((4-oxopent-2-en-1-yl)sulfonyl)-3-phenylpropan-2-yl)carbamate 
• 1334324-82-1 (S,E)-benzyl (1-((4-oxopent-2-en-1-yl)thio)-3-phenylpropan-2-yl)carbamate 
• 1334325-07-3 1-((3S,5S)-5-benzyl-1,1-dioxidothiomorpholin-3-yl)propan-2-one 
• 1334325-02-8 1-((3R,5S)-5-benzyl-1,1-dioxidothiomorpholin-3-yl)propan-2-one 
• 1334324-57-0 (3S,5S)-benzyl 3-benzyl-5-(2-oxopropyl)thiomorpholine-4-carboxylate 1,1-dioxide 
• 1334324-25-2 (3S,5R)-benzyl 3-benzyl-5-(2-oxopropyl)thiomorpholine-4-carboxylate 1,1-dioxide 
• 1334324-56-9 (3S,5S)-benzyl 3-benzyl-5-(2-oxopropyl)thiomorpholine-4-carboxylate 
• 1427030-85-0 (3S,5R)-benzyl 3-benzyl-5-(2-oxopropyl)thiomorpholine-4-carboxylate 
• 1246953-02-5 2-(N-Cbz-amino)-3-phenylpropyl-triphenylphosphonium bromide 

Relevant articles and documents

N-bromosuccinimide promoted synthesis of β-amino bromides under Appel reaction condition

An efficient and facile method has been developed for the synthesis of chiral β-amino bromides from their corresponding alcohols under Appel reaction conditions. This approach allows for the deoxybromination of a variety of β-amino alcohols in excellent y

Diastereoselective control of intramolecular aza-Michael reactions using achiral catalysts

An intramolecular aza-Michael reaction with a Cbz carbamate and an enone is reported to result in 3,5-disubstituted nitrogen-containing heterocycles. Either cis or trans isomers were obtained selectively using chiral substrates and an achiral Pd (II) comp

Synthesis of 2,6-disubstituted piperazines by a diastereoselective palladium-catalyzed hydroamination reaction

(Chemical Equation Presented) A highly diastereoselective intramolecular hydroamination is the key step in a modular synthesis of 2,6-disubstituted piperazines. The requisite hydroamination substrates were prepared in excellent yields by nucleophilic disp