Cas 1609648-69-2,2-(tert-butyldimethylsilyl)-4-(4-chlorobenzoyl)-5-((4-methoxy-3,5-dimethylphenyl)sulfinyl)-N,N-dimethylimidazole-1-sulfonamide

1609648-69-2

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Basic information

Product Name: 2-(tert-butyldimethylsilyl)-4-(4-chlorobenzoyl)-5-((4-methoxy-3,5-dimethylphenyl)sulfinyl)-N,N-dimethylimidazole-1-sulfonamide
Synonyms: 2-(tert-butyldimethylsilyl)-4-(4-chlorobenzoyl)-5-((4-methoxy-3,5-dimethylphenyl)sulfinyl)-N,N-dimethylimidazole-1-sulfonamide
CAS NO:1609648-69-2
Molecular Formula:
Molecular Weight: 610.27
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: 2-(tert-butyldimethylsilyl)-4-(4-chlorobenzoyl)-5-((4-methoxy-3,5-dimethylphenyl)sulfinyl)-N,N-dimethylimidazole-1-sulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-(tert-butyldimethylsilyl)-4-(4-chlorobenzoyl)-5-((4-methoxy-3,5-dimethylphenyl)sulfinyl)-N,N-dimethylimidazole-1-sulfonamide(1609648-69-2)
EPA Substance Registry System: 2-(tert-butyldimethylsilyl)-4-(4-chlorobenzoyl)-5-((4-methoxy-3,5-dimethylphenyl)sulfinyl)-N,N-dimethylimidazole-1-sulfonamide(1609648-69-2)

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: 1609648-69-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1609648-69-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,6,4 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1609648-69:
(9*1)+(8*6)+(7*0)+(6*9)+(5*6)+(4*4)+(3*8)+(2*6)+(1*9)=202
202 % 10 = 2
So 1609648-69-2 is a valid CAS Registry Number.

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1609648-69-2Relevant academic research and scientific papers

Full functionalization of the imidazole scaffold by selective metalation and sulfoxide/magnesium exchange

Samann, Christoph,Coya, Estibaliz,Knochel, Paul

, p. 1430 - 1434 (2014/03/21)

A simple, flexible, and straightforward method for the functionalization of all the positions of the imidazole heterocycle through regioselective arylations, allylations, acylations, and additions to aldehydes is disclosed. Starting from the readily avail

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