Cas 134309-92-5,(1S,3S,3aR,6aS)-3-(1-Benzenesulfonyl-1H-indol-3-yl)-2-(2-bromo-allyl)-5-methyl-4,6-dioxo-octahydro-pyrrolo[3,4-c]pyrrole-1-carboxylic acid methyl ester

134309-92-5

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Basic information

Product Name: (1S,3S,3aR,6aS)-3-(1-Benzenesulfonyl-1H-indol-3-yl)-2-(2-bromo-allyl)-5-methyl-4,6-dioxo-octahydro-pyrrolo[3,4-c]pyrrole-1-carboxylic acid methyl ester
Synonyms:
CAS NO:134309-92-5
Molecular Formula:
Molecular Weight: 586.463
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: (1S,3S,3aR,6aS)-3-(1-Benzenesulfonyl-1H-indol-3-yl)-2-(2-bromo-allyl)-5-methyl-4,6-dioxo-octahydro-pyrrolo[3,4-c]pyrrole-1-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (1S,3S,3aR,6aS)-3-(1-Benzenesulfonyl-1H-indol-3-yl)-2-(2-bromo-allyl)-5-methyl-4,6-dioxo-octahydro-pyrrolo[3,4-c]pyrrole-1-carboxylic acid methyl ester(134309-92-5)
EPA Substance Registry System: (1S,3S,3aR,6aS)-3-(1-Benzenesulfonyl-1H-indol-3-yl)-2-(2-bromo-allyl)-5-methyl-4,6-dioxo-octahydro-pyrrolo[3,4-c]pyrrole-1-carboxylic acid methyl ester(134309-92-5)

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: 134309-92-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 134309-92-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,3,0 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 134309-92:
(8*1)+(7*3)+(6*4)+(5*3)+(4*0)+(3*9)+(2*9)+(1*2)=115
115 % 10 = 5
So 134309-92-5 is a valid CAS Registry Number.

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134309-92-5Relevant academic research and scientific papers

Sequential 1,3-dipolar cycloaddition-palladium catalysed cyclisation. A powerful new tactical combination

Grigg, Ronald,Coulter, Thomas

, p. 1359 - 1362 (1991)

A new flexible tactical combination of a 1,3-dipolar cycloaddition of an in situ generated azomethine ylide followed by a palladium catalysed cyclisation is described. The two reactions can be carried out as a 1 pot procedure if desired. Four new stereoce

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