Cas 1609582-82-2,ethyl 2,2-difluoro-2-[1-[(4-methoxyphenyl)methyl]-2-oxo-3-pyridyl]acetate

1609582-82-2

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Basic information

Product Name: ethyl 2,2-difluoro-2-[1-[(4-methoxyphenyl)methyl]-2-oxo-3-pyridyl]acetate
Synonyms: ethyl 2,2-difluoro-2-[1-[(4-methoxyphenyl)methyl]-2-oxo-3-pyridyl]acetate
CAS NO:1609582-82-2
Molecular Formula:
Molecular Weight: 337.323
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 2,2-difluoro-2-[1-[(4-methoxyphenyl)methyl]-2-oxo-3-pyridyl]acetate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 2,2-difluoro-2-[1-[(4-methoxyphenyl)methyl]-2-oxo-3-pyridyl]acetate(1609582-82-2)
EPA Substance Registry System: ethyl 2,2-difluoro-2-[1-[(4-methoxyphenyl)methyl]-2-oxo-3-pyridyl]acetate(1609582-82-2)

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: 1609582-82-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1609582-82-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,5,8 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1609582-82:
(9*1)+(8*6)+(7*0)+(6*9)+(5*5)+(4*8)+(3*2)+(2*8)+(1*2)=192
192 % 10 = 2
So 1609582-82-2 is a valid CAS Registry Number.

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1609582-82-2Relevant academic research and scientific papers

Copper-catalyzed olefinic C-H difluoroacetylation of enamides

Caillot, Gilles,Dufour, Jérémy,Belhomme, Marie-Charlotte,Poisson, Thomas,Grimaud, Laurence,Pannecoucke, Xavier,Gillaizeau, Isabelle

, p. 5887 - 5890 (2014/05/20)

Copper-catalyzed olefinic difluoroacetylation of enamides via direct C-H bond functionalization using BrCF2CO2Et is reported for the first time. It constitutes an efficient radical-free method for the regioselective synthesis of β-di

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