Cas 1609582-63-9,phenyl 5-(2-ethoxy-1,1-difluoro-2-oxoethyl)-3,4-dihydro-2H-pyridine-1-carboxylate

1609582-63-9

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Basic information

Product Name: phenyl 5-(2-ethoxy-1,1-difluoro-2-oxoethyl)-3,4-dihydro-2H-pyridine-1-carboxylate
Synonyms: phenyl 5-(2-ethoxy-1,1-difluoro-2-oxoethyl)-3,4-dihydro-2H-pyridine-1-carboxylate
CAS NO:1609582-63-9
Molecular Formula:
Molecular Weight: 325.312
EINECS: N/A
Product Categories: N/A
Mol File: 1609582-63-9.mol
Article Data: 2

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: phenyl 5-(2-ethoxy-1,1-difluoro-2-oxoethyl)-3,4-dihydro-2H-pyridine-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: phenyl 5-(2-ethoxy-1,1-difluoro-2-oxoethyl)-3,4-dihydro-2H-pyridine-1-carboxylate(1609582-63-9)
EPA Substance Registry System: phenyl 5-(2-ethoxy-1,1-difluoro-2-oxoethyl)-3,4-dihydro-2H-pyridine-1-carboxylate(1609582-63-9)

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: 1609582-63-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1609582-63-9 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, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1609582-63:
(9*1)+(8*6)+(7*0)+(6*9)+(5*5)+(4*8)+(3*2)+(2*6)+(1*3)=189
189 % 10 = 9
So 1609582-63-9 is a valid CAS Registry Number.

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1609582-63-9Relevant articles and documents

Iron catalyzed β-C(sp2)-H alkylation of enamides

Bertho, Sylvain,Maazaoui, Radhouan,Torun, Damla,Dondasse, Isma?l,Abderrahim, Raoudha,Nicolas, Cyril,Gillaizeau, Isabelle

, p. 17475 - 17482 (2021/10/04)

An attractive and cheap alternative approach was developed for the β-C(sp2)-H (fluoro)alkylation of a range of cyclic and acyclic non-aromatic enamides using either FeCl2as a catalyst or a stoichiometric amount of nontoxic iron powder. This reaction is regioselective and exhibits broad substrate scope and good functional group tolerance.

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