Cas 1194552-09-4,N-(4-(N-((2-(p-tolylamino)thiazol-5-yl)methyl)sulfamoyl)benzyl)acetamide

1194552-09-4

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Basic information

Product Name: N-(4-(N-((2-(p-tolylamino)thiazol-5-yl)methyl)sulfamoyl)benzyl)acetamide
Synonyms: N-(4-(N-((2-(p-tolylamino)thiazol-5-yl)methyl)sulfamoyl)benzyl)acetamide
CAS NO:1194552-09-4
Molecular Formula:
Molecular Weight: 430.552
EINECS: N/A
Product Categories: N/A
Mol File: 1194552-09-4.mol
Article Data: 1

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-(4-(N-((2-(p-tolylamino)thiazol-5-yl)methyl)sulfamoyl)benzyl)acetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(4-(N-((2-(p-tolylamino)thiazol-5-yl)methyl)sulfamoyl)benzyl)acetamide(1194552-09-4)
EPA Substance Registry System: N-(4-(N-((2-(p-tolylamino)thiazol-5-yl)methyl)sulfamoyl)benzyl)acetamide(1194552-09-4)

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: 1194552-09-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1194552-09-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,4,5,5 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1194552-09:
(9*1)+(8*1)+(7*9)+(6*4)+(5*5)+(4*5)+(3*2)+(2*0)+(1*9)=164
164 % 10 = 4
So 1194552-09-4 is a valid CAS Registry Number.

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1194552-09-4Relevant articles and documents

Nucleophilic capture of the imino-quinone methide type intermediates generated from 2-aminothiazol-5-yl carbinols

Saulnier, Mark G.,Dodier, Marco,Frennesson, David B.,Langley, David R.,Vyas, Dolatrai M.

supporting information; experimental part, p. 5154 - 5157 (2009/12/28)

Generation of imino-quinone methide type intermediates from 2-aminothiazole-5-carbinols using alkylsulfonic acids in nitromethane followed by trapping with a wide range of nucleophiles effects C-C, C-O, C-N, C-S, and C-P bond formation

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