Cas 1246403-47-3,N-[N-(p-toluenesulfonyl)-p-nitrobenzenesulfonimidoyl]-7-azabicyclo[4.1.0]heptane

1246403-47-3

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Basic information

Product Name: N-[N-(p-toluenesulfonyl)-p-nitrobenzenesulfonimidoyl]-7-azabicyclo[4.1.0]heptane
Synonyms: N-[N-(p-toluenesulfonyl)-p-nitrobenzenesulfonimidoyl]-7-azabicyclo[4.1.0]heptane
CAS NO:1246403-47-3
Molecular Formula:
Molecular Weight: 435.525
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: N-[N-(p-toluenesulfonyl)-p-nitrobenzenesulfonimidoyl]-7-azabicyclo[4.1.0]heptane(CAS DataBase Reference)
NIST Chemistry Reference: N-[N-(p-toluenesulfonyl)-p-nitrobenzenesulfonimidoyl]-7-azabicyclo[4.1.0]heptane(1246403-47-3)
EPA Substance Registry System: N-[N-(p-toluenesulfonyl)-p-nitrobenzenesulfonimidoyl]-7-azabicyclo[4.1.0]heptane(1246403-47-3)

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: 1246403-47-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1246403-47-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,6,4,0 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1246403-47:
(9*1)+(8*2)+(7*4)+(6*6)+(5*4)+(4*0)+(3*3)+(2*4)+(1*7)=133
133 % 10 = 3
So 1246403-47-3 is a valid CAS Registry Number.

1246403-47-3Upstream product

1246403-47-3Downstream Products

1246403-47-3Relevant academic research and scientific papers

Catalytic stereoselective alkene aziridination with sulfonimidamides

Robert-Peillard, Fabien,Di Chenna, Pablo H.,Liang, Chungen,Lescot, Camille,Collet, Florence,Dodd, Robert H.,Dauban, Philippe

experimental part, p. 1447 - 1457 (2010/11/04)

Diastereoselective copper-catalyzed alkene aziridination has been investigated using chiral nitrenes generated from sulfonimidamides in the presence of an iodine(III) oxidant. Starting from a stoichiometric amount of the substrates, the corresponding azir

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