Cas 1044166-02-0,1-ethyl-5-[(2E)-3-(4-bromophenyl)prop-2-enoyl]-4-phenyl-3,4-dihydropyrimidin-2(1H)-one

1044166-02-0

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Basic information

Product Name: 1-ethyl-5-[(2E)-3-(4-bromophenyl)prop-2-enoyl]-4-phenyl-3,4-dihydropyrimidin-2(1H)-one
Synonyms: 1-ethyl-5-[(2E)-3-(4-bromophenyl)prop-2-enoyl]-4-phenyl-3,4-dihydropyrimidin-2(1H)-one
CAS NO:1044166-02-0
Molecular Formula:
Molecular Weight: 411.298
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-ethyl-5-[(2E)-3-(4-bromophenyl)prop-2-enoyl]-4-phenyl-3,4-dihydropyrimidin-2(1H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-ethyl-5-[(2E)-3-(4-bromophenyl)prop-2-enoyl]-4-phenyl-3,4-dihydropyrimidin-2(1H)-one(1044166-02-0)
EPA Substance Registry System: 1-ethyl-5-[(2E)-3-(4-bromophenyl)prop-2-enoyl]-4-phenyl-3,4-dihydropyrimidin-2(1H)-one(1044166-02-0)

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: 1044166-02-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1044166-02-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,4,1,6 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1044166-02:
(9*1)+(8*0)+(7*4)+(6*4)+(5*1)+(4*6)+(3*6)+(2*0)+(1*2)=110
110 % 10 = 0
So 1044166-02-0 is a valid CAS Registry Number.

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1044166-02-0Relevant academic research and scientific papers

5-Cinnamoyl- and 5-(ethoxycarbonyl)-6-styryl derivatives of 4-aryl-3,4-dihydropyrimidin-2(1H)-ones

Kolosov, Maksim A.,Orlov, Valeriy D.,Vashchenko, Valeriy V.,Shishkina, Svetlana V.,Shishkin, Oleg V.

, p. 1219 - 1228 (2007)

Several 5-cinnamoyl- and 5-(ethoxycarbonyl)-6-styryl derivatives of 4-aryl-3,4-dihydropyrimidin-2(1H)-ones were obtained and their physicochemical properties were investigated. The introduction of alkyl substituent in position 1 of dihydropyrimidine ring

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