Cas 1634721-15-5,2-(3-oxo-1,2-benzothiazol-2(3H)-yl)-N-(5-(4-pentylphenyl)-1,3,4-thiadiazol-2-yl)acetamide

1634721-15-5

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Basic information

Product Name: 2-(3-oxo-1,2-benzothiazol-2(3H)-yl)-N-(5-(4-pentylphenyl)-1,3,4-thiadiazol-2-yl)acetamide
Synonyms: 2-(3-oxo-1,2-benzothiazol-2(3H)-yl)-N-(5-(4-pentylphenyl)-1,3,4-thiadiazol-2-yl)acetamide
CAS NO:1634721-15-5
Molecular Formula:
Molecular Weight: 438.574
EINECS: N/A
Product Categories: N/A
Mol File: 1634721-15-5.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: 2-(3-oxo-1,2-benzothiazol-2(3H)-yl)-N-(5-(4-pentylphenyl)-1,3,4-thiadiazol-2-yl)acetamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-(3-oxo-1,2-benzothiazol-2(3H)-yl)-N-(5-(4-pentylphenyl)-1,3,4-thiadiazol-2-yl)acetamide(1634721-15-5)
EPA Substance Registry System: 2-(3-oxo-1,2-benzothiazol-2(3H)-yl)-N-(5-(4-pentylphenyl)-1,3,4-thiadiazol-2-yl)acetamide(1634721-15-5)

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: 1634721-15-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1634721-15-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,3,4,7,2 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1634721-15:
(9*1)+(8*6)+(7*3)+(6*4)+(5*7)+(4*2)+(3*1)+(2*1)+(1*5)=155
155 % 10 = 5
So 1634721-15-5 is a valid CAS Registry Number.

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1634721-15-5Relevant articles and documents

Synthesis of N-(5-aryl-1,3,4-thiadiazol-2-yl)-2-(3-oxo-1,2-benzothiazol- 2(3H)-yl)acetamide derivatives promoted by carbodiimide condensation

Yu, Peng,Hu, Jun,Wan, Rong,Li, Xi,Zheng, Shanlong,Xu, Yanhua

, p. 347 - 350 (2014/07/08)

Novel N-(5-aryl-1,3,4-thiadiazol-2-yl)-2-(3-oxo-1,2-benzothiazol-2(3H)-yl) acetamide derivatives were prepared by 1-(3-dimethylaminopropyl)-3- ethylcarbodiimide hydrochloride and N-hydroxybenzotrizole condensation catalysis in a convenient and fast method

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