Cas 126028-04-4,(1S,3R,3aS,6aR)-1,5-Dimethyl-4,6-dioxo-3-phenyl-octahydro-pyrrolo[3,4-c]pyrrole-1-carboxylic acid

126028-04-4

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Basic information

Product Name: (1S,3R,3aS,6aR)-1,5-Dimethyl-4,6-dioxo-3-phenyl-octahydro-pyrrolo[3,4-c]pyrrole-1-carboxylic acid
Synonyms:
CAS NO:126028-04-4
Molecular Formula:
Molecular Weight: 288.303
EINECS: N/A
Product Categories: N/A
Mol File: 126028-04-4.mol
Article Data: 1

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: (1S,3R,3aS,6aR)-1,5-Dimethyl-4,6-dioxo-3-phenyl-octahydro-pyrrolo[3,4-c]pyrrole-1-carboxylic acid(CAS DataBase Reference)
NIST Chemistry Reference: (1S,3R,3aS,6aR)-1,5-Dimethyl-4,6-dioxo-3-phenyl-octahydro-pyrrolo[3,4-c]pyrrole-1-carboxylic acid(126028-04-4)
EPA Substance Registry System: (1S,3R,3aS,6aR)-1,5-Dimethyl-4,6-dioxo-3-phenyl-octahydro-pyrrolo[3,4-c]pyrrole-1-carboxylic acid(126028-04-4)

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: 126028-04-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 126028-04-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,0,2 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 126028-04:
(8*1)+(7*2)+(6*6)+(5*0)+(4*2)+(3*8)+(2*0)+(1*4)=94
94 % 10 = 4
So 126028-04-4 is a valid CAS Registry Number.

126028-04-4Upstream product

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126028-04-4Relevant articles and documents

DECARBOXYLATION OF α-AMINO ACIDS BY PYRUVIC ACID AND ITS DERIVATIVES. EVIDENCE FOR AZOMETHINE YLIDES IN IN VITRO ANALOGUES OF PYRUVOYL ENZYMIC PROCESSES

Grigg, Ronald,Henderson, Deirdre,Hudson, Andrew J.

, p. 2841 - 2844 (2007/10/02)

Reaction of α-amino acids with pyruvic acid, ethyl pyruvate or pyruvamide in hot DMF results in imine formation followed by decarboxylation to generate azomethine ylides stereospecifically.The azomethine ylides undergo stereospecific cycloaddition to N-me

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