Cas 123932-18-3,(S)-2-[(3S,4R)-2-Oxo-3-((S)-2-oxo-4-phenyl-oxazolidin-3-yl)-4-phenyl-azetidin-1-yl]-succinic acid 1-tert-butyl ester 4-ethyl ester

123932-18-3

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Basic information

Product Name: (S)-2-[(3S,4R)-2-Oxo-3-((S)-2-oxo-4-phenyl-oxazolidin-3-yl)-4-phenyl-azetidin-1-yl]-succinic acid 1-tert-butyl ester 4-ethyl ester
Synonyms: (S)-2-[(3S,4R)-2-Oxo-3-((S)-2-oxo-4-phenyl-oxazolidin-3-yl)-4-phenyl-azetidin-1-yl]-succinic acid 1-tert-butyl ester 4-ethyl ester
CAS NO:123932-18-3
Molecular Formula:
Molecular Weight: 508.571
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (S)-2-[(3S,4R)-2-Oxo-3-((S)-2-oxo-4-phenyl-oxazolidin-3-yl)-4-phenyl-azetidin-1-yl]-succinic acid 1-tert-butyl ester 4-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-[(3S,4R)-2-Oxo-3-((S)-2-oxo-4-phenyl-oxazolidin-3-yl)-4-phenyl-azetidin-1-yl]-succinic acid 1-tert-butyl ester 4-ethyl ester(123932-18-3)
EPA Substance Registry System: (S)-2-[(3S,4R)-2-Oxo-3-((S)-2-oxo-4-phenyl-oxazolidin-3-yl)-4-phenyl-azetidin-1-yl]-succinic acid 1-tert-butyl ester 4-ethyl ester(123932-18-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 123932-18-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 123932-18-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,9,3 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 123932-18:
(8*1)+(7*2)+(6*3)+(5*9)+(4*3)+(3*2)+(2*1)+(1*8)=113
113 % 10 = 3
So 123932-18-3 is a valid CAS Registry Number.

123932-18-3Upstream product

123932-18-3Downstream Products

123932-18-3Relevant academic research and scientific papers

Asymmetric alkylations of a phenylalanylglycinate equivalent. Novel route to dipeptides bearing α-alkyl-α-amino acid residues

Ojima,Komata,Qiu

, p. 770 - 774 (2007/10/02)

Asymmetric single and double alkylations of chiral β-lactam acetate 1, which is a chiral glycinate as well as a phenylalanylglycinate equivalent, are studied. First, the sequential asymmetric double alkylation of 1a is performed to give the corresponding

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