Cas 237421-75-9,(2S,4S)-4-(2-Methoxycarbonyl-2-oxo-ethyl)-5-oxo-pyrrolidine-1,2-dicarboxylic acid 2-benzyl ester 1-tert-butyl ester

237421-75-9

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Basic information

Product Name: (2S,4S)-4-(2-Methoxycarbonyl-2-oxo-ethyl)-5-oxo-pyrrolidine-1,2-dicarboxylic acid 2-benzyl ester 1-tert-butyl ester
Synonyms:
CAS NO:237421-75-9
Molecular Formula:
Molecular Weight: 419.431
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: (2S,4S)-4-(2-Methoxycarbonyl-2-oxo-ethyl)-5-oxo-pyrrolidine-1,2-dicarboxylic acid 2-benzyl ester 1-tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,4S)-4-(2-Methoxycarbonyl-2-oxo-ethyl)-5-oxo-pyrrolidine-1,2-dicarboxylic acid 2-benzyl ester 1-tert-butyl ester(237421-75-9)
EPA Substance Registry System: (2S,4S)-4-(2-Methoxycarbonyl-2-oxo-ethyl)-5-oxo-pyrrolidine-1,2-dicarboxylic acid 2-benzyl ester 1-tert-butyl ester(237421-75-9)

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: 237421-75-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 237421-75-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,7,4,2 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 237421-75:
(8*2)+(7*3)+(6*7)+(5*4)+(4*2)+(3*1)+(2*7)+(1*5)=129
129 % 10 = 9
So 237421-75-9 is a valid CAS Registry Number.

237421-75-9Upstream product

113400-36-5 benzyl (2S)-N-tert-butoxycarbonyl-5-oxoprolinate

237421-75-9Downstream Products

237421-75-9Relevant academic research and scientific papers

Versatile synthesis of inhibitors of late enzymes in the bacterial pathway to lysine

Steger, Matthias,Young, Douglas W.

, p. 7935 - 7956 (1999)

Modification of our 'ring switching' reaction has allowed us to develop a versatile synthesis of potential inhibitors of the late enzymes in the bacterial pathway to lysine. The methodology is applicable to solid phase combinatorial synthesis.

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