83160-23-0

Basic information

• Product Name: Benzeneacetic acid, a-[[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-2-propenyl]amino]- 4-(phenylmethoxy)-, methyl ester, (R)-
• CAS NO: 83160-23-0
• Molecular Formula: C27H22N2O6
• Molecular Weight: 470.481
• Mol File: 83160-23-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzeneacetic acid, a-[[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-2-propenyl]amino]- 4-(phenylmethoxy)-, methyl ester, (R)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetic acid, a-[[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-2-propenyl]amino]- 4-(phenylmethoxy)-, methyl ester, (R)-(83160-23-0)
• EPA Substance Registry System: Benzeneacetic acid, a-[[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-2-propenyl]amino]- 4-(phenylmethoxy)-, methyl ester, (R)-(83160-23-0)

Safety Data

• Hazardous Substances Data: 83160-23-0(Hazardous Substances Data)

Upstream product

• 88143-74-2 (R)-1-(4-(benzyloxy)phenyl)-2-methoxy-2-oxoethan-1-aminium chloride 
• 29588-89-4 (2S)-2-(1,3-dioxoisoindolin-2-yl)-3-hydroxypropanoic acid 
• 78246-50-1 methyl (L)-N^α-phthaloylseryl-(D)-p-benzyloxyphenylglycinate 
• 71336-83-9 methyl D-(p-benzyloxyphenyl)glycinate 
• 29588-89-4 N-phthaloyl-L-serine 
• 83160-21-8 (R)-(4-Benzyloxy-phenyl)-[(S)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-methanesulfonyloxy-propionylamino]-acetic acid methyl ester 
• 78246-50-1 (R)-(4-Benzyloxy-phenyl)-[(R)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-hydroxy-propionylamino]-acetic acid methyl ester 

Relevant articles and documents

Nocardicin A: Stereochemical and Biomimetic Studies of Monocyclic β-Lactam Formation

Using 3H/14C doubly labeled specimens of L- and D-serine bearing tritium label at C-2, biosynthetic studies of norcardicin A (1) produced by whole cells of Nocardia uniformis subsp. tsuyamanensis (ATCC 21806) are reported that indicate (a) that D-serine i

IMPROVED ASYMMETRIC SYNTHESIS OF (-)-3-AMINOCARDICINIC ACID AND FURTHER OBSERVATIONS OF THE MITSUNOBU REACTION FOR β-LACTAM FORMATION IN SERYL PEPTIDES

Protected seryl peptide 2 was treated under a variety of conditions with triphenylphosphine or triethylphosphine and diethyl azodicarboxylate to give mechanistic insight into the β-lactam forming reaction and an improved route to (-)-3-aminocardicinic aci