72015-61-3

Basic information

• Product Name: 2-Propenoic acid, 3-phenyl-2-[[(phenylmethoxy)carbonyl]amino]-, (Z)-
• CAS NO: 72015-61-3
• Molecular Formula: C17H15NO4
• Molecular Weight: 297.31
• Mol File: 72015-61-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-Propenoic acid, 3-phenyl-2-[[(phenylmethoxy)carbonyl]amino]-, (Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenoic acid, 3-phenyl-2-[[(phenylmethoxy)carbonyl]amino]-, (Z)-(72015-61-3)
• EPA Substance Registry System: 2-Propenoic acid, 3-phenyl-2-[[(phenylmethoxy)carbonyl]amino]-, (Z)-(72015-61-3)

Safety Data

• Hazardous Substances Data: 72015-61-3(Hazardous Substances Data)

Upstream product

• 621-84-1 O-benzyl carbamate 
• 156-06-9 2-oxo-3-(phenyl)propionic acid 
• 50685-12-6 N-<(Carbobenzyl)oxy>-Δ^E-phenylalanine Ethyl Ester 
• 50685-13-7 ethyl (Z)-α-N-benzyloxycarbonyl-α,β-didehydrophenylalaninate 
• 71663-73-5 β-Aminozimtsaeureethylester 
• 77416-48-9 (Z)-2-Azidocarbonyl-3-phenyl-acrylic acid ethyl ester 
• 100-51-6 benzyl alcohol 
• 24302-10-1 2-[1-phenyl-(Z)-methylidene]malonic acid monoethyl ester 
• 5817-49-2 (αRS,βRS)-N-[(benzyloxy)carbonyl]-β-hydroxy-phenylalanine 
• 5817-49-2 N-benzyloxycarbonyl-DL-erythro-β-phenylserine 
• 73087-17-9 2-benzyloxy-4-benzyl-DL-oxazol-5(4H)-one 
• 501-53-1 benzyl chloroformate 
• 6613-41-8 ethyl 3-phenylpyruvate 
• 74805-39-3 (Z)-2-benzyloxy-4-benzylideneoxazol-5-one 

Downstream Products

• 1373888-75-5 ethyl (Z)-2-[1-(((benzyloxy)carbonyl)amino)-2-phenylethen-1-yl]oxazole-4-carboxylate 
• 1373888-82-4 (Z)-2-((benzyloxy)carbonyl)amino-3-phenyl-2-propenamide 
• 84759-71-7 1, D-Ala², Leu⁵-OMe>Enkephalin 
• 38155-45-2 methyl L-phenylalanyl-L-leucinate hydrochloride 
• 3850-44-0 (D,L)-CBZ-Phe-Leu-OMe 
• 3850-45-1 Cbz-L-Phe-L-Leu-OMe 
• 3338-39-4 (R)-2-((R)-2-Benzyloxycarbonylamino-3-phenyl-propionylamino)-propionic acid 
• 101105-20-8 N-cyclohexyl-2-oxo-3-phenylpropanamide 
• 851219-56-2 S-methoxybenzyl-N-carbobenzyloxy-β-phenylcysteine methyl ester 
• 99075-75-9 threo-β-phenylcysteine methyl ester hydrochloride 

Relevant articles and documents

PREPARATION OF ALL THE FOUR DIASTEREOMERS OF β-PHENYLCYSTEINE METHYL ESTER THROUGH CHROMATOGRAPHIC OPTICAL RESOLUTION OF THE 2,2-DIMETHYLTHIAZOLIDINE DERIVATIVES

cis- And trans-2,2-dimethyl-4-carbomethoxy-5-phenylthiazolidines prepared from the corresponding erythro- and threo-β-phenylcysteines were resolved into the enantiomers by use of a chiral HPLC column, from which all of the four chiral β-phenylcysteine met

THE SYNTHESES OF N-FREE α-DEHYDROAMINO ACID ESTERS AND N-ACETYL DEHYDRODIPEPTIDE ESTER FROM N-CARBOXY α-DEHYDROAMINO ACID ANHYDRIDE

N-Carboxy α-dehydroamino acid anhydride, derived from N-benzyloxycarbonyl α-dehydroamino acid (DHA) and thionyl chloride, was found to be very useful for the synthesis of N-free DHA ester by alcoholysis and N-acetyl dehydrodipeptide ester by coupling was

Dehydrooligopeptides. I. The facile coupling of α-amino acids with α-dehydroamino acids to dehydrodipeptides

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