Cas 1214914-22-3,6-(difluoro(phenyl)methyl)-4-(ethoxycarbonylmethyl)-3-phenyl-3,4-dihydropyrimidin-2(1H)-one

1214914-22-3

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Basic information

Product Name: 6-(difluoro(phenyl)methyl)-4-(ethoxycarbonylmethyl)-3-phenyl-3,4-dihydropyrimidin-2(1H)-one
Synonyms: 6-(difluoro(phenyl)methyl)-4-(ethoxycarbonylmethyl)-3-phenyl-3,4-dihydropyrimidin-2(1H)-one
CAS NO:1214914-22-3
Molecular Formula:
Molecular Weight: 386.398
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: 6-(difluoro(phenyl)methyl)-4-(ethoxycarbonylmethyl)-3-phenyl-3,4-dihydropyrimidin-2(1H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 6-(difluoro(phenyl)methyl)-4-(ethoxycarbonylmethyl)-3-phenyl-3,4-dihydropyrimidin-2(1H)-one(1214914-22-3)
EPA Substance Registry System: 6-(difluoro(phenyl)methyl)-4-(ethoxycarbonylmethyl)-3-phenyl-3,4-dihydropyrimidin-2(1H)-one(1214914-22-3)

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: 1214914-22-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1214914-22-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,4,9,1 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1214914-22:
(9*1)+(8*2)+(7*1)+(6*4)+(5*9)+(4*1)+(3*4)+(2*2)+(1*2)=123
123 % 10 = 3
So 1214914-22-3 is a valid CAS Registry Number.

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1214914-22-3Relevant academic research and scientific papers

A new strategy for the synthesis of fluorinated 3,4-dihydropyrimidinones

Fustero, Santos,Catalán, Silvia,Ace?a, José Luis,del Pozo, Carlos

experimental part, p. 1145 - 1150 (2010/03/01)

A new family of 3,4-dihydropyrimidinones (DHPMs) bearing fluorinated substituents at C6 have been prepared from gem-difluorinated nitriles, alkyl 3-butenoates and iso(thio)cyanates. This novel Biginelli-type process relies on the γ-addition of the ester-derived enolate to fluorinated nitriles. A tandem nucleophilic addition aza-Michael reaction sequence completes the synthetic process.

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