Cas 1372799-00-2,1-(2-(N-(2-(2,4,4-trimethylpentan-2-ylcarbamoyl)propan-2-yl)-N-ethylcarbamoyl)phenyl)-3-(4-methoxyphenyl)urea

1372799-00-2

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Basic information

Product Name: 1-(2-(N-(2-(2,4,4-trimethylpentan-2-ylcarbamoyl)propan-2-yl)-N-ethylcarbamoyl)phenyl)-3-(4-methoxyphenyl)urea
Synonyms:
CAS NO:1372799-00-2
Molecular Formula:
Molecular Weight: 510.677
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: 1-(2-(N-(2-(2,4,4-trimethylpentan-2-ylcarbamoyl)propan-2-yl)-N-ethylcarbamoyl)phenyl)-3-(4-methoxyphenyl)urea(CAS DataBase Reference)
NIST Chemistry Reference: 1-(2-(N-(2-(2,4,4-trimethylpentan-2-ylcarbamoyl)propan-2-yl)-N-ethylcarbamoyl)phenyl)-3-(4-methoxyphenyl)urea(1372799-00-2)
EPA Substance Registry System: 1-(2-(N-(2-(2,4,4-trimethylpentan-2-ylcarbamoyl)propan-2-yl)-N-ethylcarbamoyl)phenyl)-3-(4-methoxyphenyl)urea(1372799-00-2)

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: 1372799-00-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1372799-00-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,2,7,9 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1372799-00:
(9*1)+(8*3)+(7*7)+(6*2)+(5*7)+(4*9)+(3*9)+(2*0)+(1*0)=192
192 % 10 = 2
So 1372799-00-2 is a valid CAS Registry Number.

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1372799-00-2Relevant academic research and scientific papers

Efficient synthesis of urea derivatives via a sequential one-pot nucleophilic addition/Ugi five-component reaction under solvent-free conditions

Azizian, Javad,Yadollahzadeh, Khadijeh,Tahermansouri, Hasan,Khoei, Davood Chobfrosh,Delbari, Akram Sadat

, p. 2110 - 2120 (2012/06/04)

Urea polyfunctional derivatives were successfully synthesized via a one-pot, five-component nucleophilic addition/Ugi reaction sequence. Simplicity, solvent-free conditions, and good yields of products are advantages of this method.

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