Cas 127253-92-3,(1S,3aR,6aS)-4,6-Dioxo-5-phenyl-2-((R)-1-phenyl-2-trimethylsilanyloxy-ethyl)-octahydro-pyrrolo[3,4-c]pyrrole-1-carbonitrile

127253-92-3

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Basic information

Product Name: (1S,3aR,6aS)-4,6-Dioxo-5-phenyl-2-((R)-1-phenyl-2-trimethylsilanyloxy-ethyl)-octahydro-pyrrolo[3,4-c]pyrrole-1-carbonitrile
Synonyms:
CAS NO:127253-92-3
Molecular Formula:
Molecular Weight: 433.582
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,3aR,6aS)-4,6-Dioxo-5-phenyl-2-((R)-1-phenyl-2-trimethylsilanyloxy-ethyl)-octahydro-pyrrolo[3,4-c]pyrrole-1-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: (1S,3aR,6aS)-4,6-Dioxo-5-phenyl-2-((R)-1-phenyl-2-trimethylsilanyloxy-ethyl)-octahydro-pyrrolo[3,4-c]pyrrole-1-carbonitrile(127253-92-3)
EPA Substance Registry System: (1S,3aR,6aS)-4,6-Dioxo-5-phenyl-2-((R)-1-phenyl-2-trimethylsilanyloxy-ethyl)-octahydro-pyrrolo[3,4-c]pyrrole-1-carbonitrile(127253-92-3)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 127253-92-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 127253-92-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,2,5 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 127253-92:
(8*1)+(7*2)+(6*7)+(5*2)+(4*5)+(3*3)+(2*9)+(1*2)=123
123 % 10 = 3
So 127253-92-3 is a valid CAS Registry Number.

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127253-92-3Relevant academic research and scientific papers

Asymmetric Synthesis XVII : Facile Generation of a Chiral Azomethine Ylide via the CN(R,S) Method

Rouden, Jacques,Royer, Jacques,Husson, Henri-Philippe

, p. 5133 - 5136 (2007/10/02)

(-)-N-cyanomethyl-4-phenyl-1,3-oxazolidine, prepared in one step from R-(-)-phenylglycinol, gives a chiral azomethine ylide on treatment with TMSOTf and (iPr)2NEt.This ylide undergoes 1,3-dipolar cycloaddition reactions with activated olefins under very m

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