Cas 433932-38-8,tert-butyl (2S,4RS)-N-tert-butoxycarbonyl-4-benzyloxycarbonylmethylpyroglutamate

433932-38-8

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Basic information

Product Name: tert-butyl (2S,4RS)-N-tert-butoxycarbonyl-4-benzyloxycarbonylmethylpyroglutamate
Synonyms:
CAS NO:433932-38-8
Molecular Formula:
Molecular Weight: 433.502
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: tert-butyl (2S,4RS)-N-tert-butoxycarbonyl-4-benzyloxycarbonylmethylpyroglutamate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (2S,4RS)-N-tert-butoxycarbonyl-4-benzyloxycarbonylmethylpyroglutamate(433932-38-8)
EPA Substance Registry System: tert-butyl (2S,4RS)-N-tert-butoxycarbonyl-4-benzyloxycarbonylmethylpyroglutamate(433932-38-8)

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: 433932-38-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 433932-38-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,3,9,3 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 433932-38:
(8*4)+(7*3)+(6*3)+(5*9)+(4*3)+(3*2)+(2*3)+(1*8)=148
148 % 10 = 8
So 433932-38-8 is a valid CAS Registry Number.

433932-38-8Upstream product

433932-38-8Downstream Products

433932-38-8Relevant academic research and scientific papers

Synthesis of homochiral amino acid pyrazine and pyrrole analogues of glutamate antagonists

Dinsmore, Andrew,Doyle, Paul M.,Steger, Matthias,Young, Douglas W.

, p. 613 - 621 (2007/10/03)

Use of the acid 7 and the aldehydes 23a and 23b in "ring switching" reactions with hydrazines has given β-(1-aminopyrrole)amino acids as kinetic products. The products from the reaction of the aldehyde have been converted into β-(pyrazine)amino acids by a

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