Cas 197656-99-8,4-Chloro-N-(5,6-dimethyl-1,3-dihydro-benzoimidazol-2-ylidene)-2-mercapto-5-methyl-benzenesulfonamide

197656-99-8

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Basic information

Product Name: 4-Chloro-N-(5,6-dimethyl-1,3-dihydro-benzoimidazol-2-ylidene)-2-mercapto-5-methyl-benzenesulfonamide
Synonyms:
CAS NO:197656-99-8
Molecular Formula:
Molecular Weight: 381.907
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: 4-Chloro-N-(5,6-dimethyl-1,3-dihydro-benzoimidazol-2-ylidene)-2-mercapto-5-methyl-benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-Chloro-N-(5,6-dimethyl-1,3-dihydro-benzoimidazol-2-ylidene)-2-mercapto-5-methyl-benzenesulfonamide(197656-99-8)
EPA Substance Registry System: 4-Chloro-N-(5,6-dimethyl-1,3-dihydro-benzoimidazol-2-ylidene)-2-mercapto-5-methyl-benzenesulfonamide(197656-99-8)

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: 197656-99-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 197656-99-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,6,5 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 197656-99:
(8*1)+(7*9)+(6*7)+(5*6)+(4*5)+(3*6)+(2*9)+(1*9)=208
208 % 10 = 8
So 197656-99-8 is a valid CAS Registry Number.

197656-99-8Upstream product

3171-45-7 4,5-dimethyl-1,2-phenylenediamine

197656-99-8Downstream Products

197656-99-8Relevant academic research and scientific papers

2-mercapto-N-(azolyl)benzenesulphonamides IV. syntheses of some 4-chloro-2-mercapto-5-methyl-N-(benzimidazol-2-yl)benzenesulphonamides derivatives with potential anticancer and anti-HIV activities

Pomarnacka, Elzbieta,Brzozowski, Zdzislaw

, p. 215 - 221 (2007/10/03)

Syntheses of 4-chloro-2-mercapto-5-methyl-N-(5-R1-6-R2-benzimidazol-2 -yl)benzenesulphonamides [II-V], their disulfides [IIa-IVa] and S,N-substituted derivatives [VI-IX] were described. The probable mechanism for the reactions was suggested. The moderate anticancer activity was observed in vitro for compounds [II-IV].

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