Cas 103023-64-9,7-Methyl-5-oxo-1,2,3,5,6,7-hexahydro-indolizine-8-carboxylic acid ethyl ester

103023-64-9

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Basic information

Product Name: 7-Methyl-5-oxo-1,2,3,5,6,7-hexahydro-indolizine-8-carboxylic acid ethyl ester
Synonyms: 7-Methyl-5-oxo-1,2,3,5,6,7-hexahydro-indolizine-8-carboxylic acid ethyl ester
CAS NO:103023-64-9
Molecular Formula:
Molecular Weight: 223.272
EINECS: N/A
Product Categories: N/A
Mol File: 103023-64-9.mol
Article Data: 1

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: 7-Methyl-5-oxo-1,2,3,5,6,7-hexahydro-indolizine-8-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 7-Methyl-5-oxo-1,2,3,5,6,7-hexahydro-indolizine-8-carboxylic acid ethyl ester(103023-64-9)
EPA Substance Registry System: 7-Methyl-5-oxo-1,2,3,5,6,7-hexahydro-indolizine-8-carboxylic acid ethyl ester(103023-64-9)

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: 103023-64-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 103023-64-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,0,2 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 103023-64:
(8*1)+(7*0)+(6*3)+(5*0)+(4*2)+(3*3)+(2*6)+(1*4)=59
59 % 10 = 9
So 103023-64-9 is a valid CAS Registry Number.

103023-64-9Upstream product

103023-64-9Downstream Products

103023-64-9Relevant articles and documents

Azabicyclic Compounds Synthesis: Reactions of Cyclic β-Enaminoesters with α,β-Unsaturated Carbonyl Compounds

Brunerie, Pascal,Celerier, Jean-Pierre,Huche, Michel,Lhommet, Gerard

, p. 735 - 738 (2007/10/02)

Reactions of cyclic β-enaminoesters with α,β-unsaturated acid chlorides or esters have been studied.In all cases, N-acylation takes place and, under certain conditions, a C-alkylation also occurs leading to the formation of azabicyclic products.

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