Cas 1147735-20-3,2-(2,5-dioxoimidazolidin-4-yl)-N-(3-(4-nitrophenyl)-4-phenylthiazol-2(3H)-ylidene)acetamide

1147735-20-3

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Basic information

Product Name: 2-(2,5-dioxoimidazolidin-4-yl)-N-(3-(4-nitrophenyl)-4-phenylthiazol-2(3H)-ylidene)acetamide
Synonyms:
CAS NO:1147735-20-3
Molecular Formula:
Molecular Weight: 437.436
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-(2,5-dioxoimidazolidin-4-yl)-N-(3-(4-nitrophenyl)-4-phenylthiazol-2(3H)-ylidene)acetamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-(2,5-dioxoimidazolidin-4-yl)-N-(3-(4-nitrophenyl)-4-phenylthiazol-2(3H)-ylidene)acetamide(1147735-20-3)
EPA Substance Registry System: 2-(2,5-dioxoimidazolidin-4-yl)-N-(3-(4-nitrophenyl)-4-phenylthiazol-2(3H)-ylidene)acetamide(1147735-20-3)

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: 1147735-20-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1147735-20-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,7,7,3 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1147735-20:
(9*1)+(8*1)+(7*4)+(6*7)+(5*7)+(4*3)+(3*5)+(2*2)+(1*0)=153
153 % 10 = 3
So 1147735-20-3 is a valid CAS Registry Number.

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1147735-20-3Relevant academic research and scientific papers

Synthesis of amidine and amide derivatives and their evaluation for anti-inflammatory and analgesic activities

Sondhi, Sham M.,Singh, Jaiveer,Kumar, Ashok,Jamal, Hyder,Gupta

experimental part, p. 1010 - 1015 (2009/09/06)

A number of amidine derivatives (2a-i) have been synthesized by condensation of 2-cyanopyridine with various 3,4-diaryl-2-imino-4-thiazolines. Various amide derivatives (3a-h) were synthesized by condensation of orotic acid and hydantoin-5-acetic acid wit

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