Cas 1180657-41-3,4-(6,8-dicyano-5-imino-7-methylsulfanyl-5H-thiazolo[3,2-a]-pyridin-3-yl)-N,N-dimethylbenzenesulfonamide

1180657-41-3

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Basic information

Product Name: 4-(6,8-dicyano-5-imino-7-methylsulfanyl-5H-thiazolo[3,2-a]-pyridin-3-yl)-N,N-dimethylbenzenesulfonamide
Synonyms: 4-(6,8-dicyano-5-imino-7-methylsulfanyl-5H-thiazolo[3,2-a]-pyridin-3-yl)-N,N-dimethylbenzenesulfonamide
CAS NO:1180657-41-3
Molecular Formula:
Molecular Weight: 429.547
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-(6,8-dicyano-5-imino-7-methylsulfanyl-5H-thiazolo[3,2-a]-pyridin-3-yl)-N,N-dimethylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-(6,8-dicyano-5-imino-7-methylsulfanyl-5H-thiazolo[3,2-a]-pyridin-3-yl)-N,N-dimethylbenzenesulfonamide(1180657-41-3)
EPA Substance Registry System: 4-(6,8-dicyano-5-imino-7-methylsulfanyl-5H-thiazolo[3,2-a]-pyridin-3-yl)-N,N-dimethylbenzenesulfonamide(1180657-41-3)

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: 1180657-41-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1180657-41-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,0,6,5 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1180657-41:
(9*1)+(8*1)+(7*8)+(6*0)+(5*6)+(4*5)+(3*7)+(2*4)+(1*1)=153
153 % 10 = 3
So 1180657-41-3 is a valid CAS Registry Number.

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1180657-41-3Relevant academic research and scientific papers

Heteroaromatization with sulfonamido phenyl ethanone, part II: Synthesis of novel thiazolyl acetonitriles and thiazolyl acrylonitriles and their derivatives containing dimethylsulfonamide moiety

Hassan, Saber M.,Abdel Aal, Mahmoud M.,El-Maghraby, Ahmed A.,Bashandy, Mahmoud S.

experimental part, p. 427 - 452 (2009/10/02)

Thiazolyl acetonitrile (2) was prepared and converted to pyrazolo[5,1-c][1,2,4]triazine (5), thiazoline-4-one derivatives (10,12), thiazolo[3,2-a]pyridine (13), coumarin (14), and benzo[f]coumarin (16) derivatives through reactions with a variety of organ

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