Cas 1033221-79-2,methyl 4-[(1-benzyl-6-oxo-1,6-dihydropyridin-3-yl)methyl]benzoate

1033221-79-2

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Basic information

Product Name: methyl 4-[(1-benzyl-6-oxo-1,6-dihydropyridin-3-yl)methyl]benzoate
Synonyms: methyl 4-[(1-benzyl-6-oxo-1,6-dihydropyridin-3-yl)methyl]benzoate
CAS NO:1033221-79-2
Molecular Formula:
Molecular Weight: 333.387
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: methyl 4-[(1-benzyl-6-oxo-1,6-dihydropyridin-3-yl)methyl]benzoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 4-[(1-benzyl-6-oxo-1,6-dihydropyridin-3-yl)methyl]benzoate(1033221-79-2)
EPA Substance Registry System: methyl 4-[(1-benzyl-6-oxo-1,6-dihydropyridin-3-yl)methyl]benzoate(1033221-79-2)

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: 1033221-79-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1033221-79-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,3,2,2 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1033221-79:
(9*1)+(8*0)+(7*3)+(6*3)+(5*2)+(4*2)+(3*1)+(2*7)+(1*9)=92
92 % 10 = 2
So 1033221-79-2 is a valid CAS Registry Number.

1033221-79-2Upstream product

1033221-25-8 methyl 4-[(1-benzyl-6-oxo-1,4,5,6-tetrahydropyridin-3-yl)methyl]-3-bromobenzoate

1033221-79-2Downstream Products

1033221-79-2Relevant academic research and scientific papers

Biaryl formation from 5-(2-bromobenzyl)-substituted piperidin-2-ones via palladacycles

Satyanarayana, Gedu,Maier, Martin E.

supporting information; experimental part, p. 2361 - 2364 (2009/05/27)

(Chemical Equation Presented) The reaction of piperdin-2-ones with a 2-bromobenzyl substituent in the 5-position in the presence of a palladium catalyst leads to biaryl compounds. Their formation can be explained via initial C-H insertion of the aryl pall

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