Cas 1322089-72-4,ethyl 6-methyl-4-(4-(3-(2-phenoxyphenyl)ureido)phenyl)-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate

1322089-72-4

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Basic information

Product Name: ethyl 6-methyl-4-(4-(3-(2-phenoxyphenyl)ureido)phenyl)-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate
Synonyms: ethyl 6-methyl-4-(4-(3-(2-phenoxyphenyl)ureido)phenyl)-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate
CAS NO:1322089-72-4
Molecular Formula:
Molecular Weight: 502.594
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: ethyl 6-methyl-4-(4-(3-(2-phenoxyphenyl)ureido)phenyl)-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 6-methyl-4-(4-(3-(2-phenoxyphenyl)ureido)phenyl)-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate(1322089-72-4)
EPA Substance Registry System: ethyl 6-methyl-4-(4-(3-(2-phenoxyphenyl)ureido)phenyl)-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate(1322089-72-4)

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: 1322089-72-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1322089-72-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,2,0,8 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1322089-72:
(9*1)+(8*3)+(7*2)+(6*2)+(5*0)+(4*8)+(3*9)+(2*7)+(1*2)=134
134 % 10 = 4
So 1322089-72-4 is a valid CAS Registry Number.

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1322089-72-4Relevant academic research and scientific papers

The novel 3,4-dihydropyrimidin-2(1H)-one urea derivatives of N-aryl urea: Synthesis, anti-inflammatory, antibacterial and antifungal activity evaluation

Tale, Rajesh H.,Rodge, Atish H.,Hatnapure, Girish D.,Keche, Ashish P.

, p. 4648 - 4651 (2011/09/12)

A series of novel 3,4-dihydropyrimidin-2(1H)-one urea derivatives of biological interest were prepared by sequential Bigineli's reaction, reduction followed by reaction of resulting amines with different arylisocynates. All the synthesized (1-23) compound

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