Cas 1449219-71-9,(Z)-3-benzoyl-1-[2-fluoro-3-(4-methoxyphenyl)prop-2-en-1-yl]-5-methyl-1,2,3,4-tetrahydropyrimidine-2,4-dione

1449219-71-9

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Basic information

Product Name: (Z)-3-benzoyl-1-[2-fluoro-3-(4-methoxyphenyl)prop-2-en-1-yl]-5-methyl-1,2,3,4-tetrahydropyrimidine-2,4-dione
Synonyms:
CAS NO:1449219-71-9
Molecular Formula:
Molecular Weight: 290.294
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: (Z)-3-benzoyl-1-[2-fluoro-3-(4-methoxyphenyl)prop-2-en-1-yl]-5-methyl-1,2,3,4-tetrahydropyrimidine-2,4-dione(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-3-benzoyl-1-[2-fluoro-3-(4-methoxyphenyl)prop-2-en-1-yl]-5-methyl-1,2,3,4-tetrahydropyrimidine-2,4-dione(1449219-71-9)
EPA Substance Registry System: (Z)-3-benzoyl-1-[2-fluoro-3-(4-methoxyphenyl)prop-2-en-1-yl]-5-methyl-1,2,3,4-tetrahydropyrimidine-2,4-dione(1449219-71-9)

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: 1449219-71-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1449219-71-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,9,2,1 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1449219-71:
(9*1)+(8*4)+(7*4)+(6*9)+(5*2)+(4*1)+(3*9)+(2*7)+(1*1)=179
179 % 10 = 9
So 1449219-71-9 is a valid CAS Registry Number.

1449219-71-9Upstream product

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1449219-71-9Relevant academic research and scientific papers

Aza-michael access to fluoroalkylidene analogues of biomolecules

Prunier, Anais,Calata, Charlene,Legros, Julien,Maddaluno, Jacques,Pfund, Emmanuel,Lequeux, Thierry

, p. 8083 - 8097 (2013)

The synthesis of fluoroaminosulfones derived from piperidine and nucleic bases followed by the study of their chemical behavior in the modified Julia reaction are described. The resulting aminosulfones open a straightforward access to a series of new fluorinated biomolecules including a potent DPP-II inhibitor and acyclonucleoside analogues as potential enzyme inhibitors.

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