Cas 1133475-64-5,2-(4-chlorophenyl)-1H-benzimidazole-4-sulfonic acid benzylamide

1133475-64-5

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Basic information

Product Name: 2-(4-chlorophenyl)-1H-benzimidazole-4-sulfonic acid benzylamide
Synonyms: 2-(4-chlorophenyl)-1H-benzimidazole-4-sulfonic acid benzylamide
CAS NO:1133475-64-5
Molecular Formula:
Molecular Weight: 397.885
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-(4-chlorophenyl)-1H-benzimidazole-4-sulfonic acid benzylamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-chlorophenyl)-1H-benzimidazole-4-sulfonic acid benzylamide(1133475-64-5)
EPA Substance Registry System: 2-(4-chlorophenyl)-1H-benzimidazole-4-sulfonic acid benzylamide(1133475-64-5)

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: 1133475-64-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1133475-64-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,3,4,7 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1133475-64:
(9*1)+(8*1)+(7*3)+(6*3)+(5*4)+(4*7)+(3*5)+(2*6)+(1*4)=135
135 % 10 = 5
So 1133475-64-5 is a valid CAS Registry Number.

1133475-64-5Upstream product

104-88-1 4-chlorobenzaldehyde

1133475-64-5Downstream Products

1133475-64-5Relevant academic research and scientific papers

A general method for the synthesis of benzimidazole-4-sulfonamides

Rosen, Mark D.,Simon, Zahna M.,Tarantino, Kyle T.,Zhao, Lucy X.,Rabinowitz, Michael H.

, p. 1219 - 1221 (2009)

A general method for the synthesis of benzimidazole-4-sulfonamides is described. This methodology employs commercially available benzothiadiazole-4-sulfonyl chloride as a benzimidazole equivalent. Reaction with a variety of amines followed by highly chemo

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