Cas 1261165-52-9,(E)-tert-butyl 3-(1-benzyl-4-oxo-1,4-dihydroquinolin-3-yl)acrylate

1261165-52-9

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Basic information

Product Name: (E)-tert-butyl 3-(1-benzyl-4-oxo-1,4-dihydroquinolin-3-yl)acrylate
Synonyms: (E)-tert-butyl 3-(1-benzyl-4-oxo-1,4-dihydroquinolin-3-yl)acrylate
CAS NO:1261165-52-9
Molecular Formula:
Molecular Weight: 361.441
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: (E)-tert-butyl 3-(1-benzyl-4-oxo-1,4-dihydroquinolin-3-yl)acrylate(CAS DataBase Reference)
NIST Chemistry Reference: (E)-tert-butyl 3-(1-benzyl-4-oxo-1,4-dihydroquinolin-3-yl)acrylate(1261165-52-9)
EPA Substance Registry System: (E)-tert-butyl 3-(1-benzyl-4-oxo-1,4-dihydroquinolin-3-yl)acrylate(1261165-52-9)

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: 1261165-52-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1261165-52-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,1,1,6 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1261165-52:
(9*1)+(8*2)+(7*6)+(6*1)+(5*1)+(4*6)+(3*5)+(2*5)+(1*2)=129
129 % 10 = 9
So 1261165-52-9 is a valid CAS Registry Number.

1261165-52-9Upstream product

1261165-52-9Downstream Products

1261165-52-9Relevant academic research and scientific papers

Palladium-catalyzed dehydrogenation/oxidative cross-coupling sequence of β-heteroatom-substituted ketones

Moon, Youngtaek,Kwon, Daeil,Hong, Sungwoo

supporting information, p. 11333 - 11336,4 (2012/12/12)

Concise and selective: The title one-pot sequence allows formation of the enone functionality and subsequent cross-coupling. The process provides access to highly functionalized cyclic enolones and enaminones from readily accessible β-heteroatom-substitut

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