Cas 127452-95-3,3-Cyclohexene-1-carboxylic acid, 1-(2-bromoethyl)-3-methoxy-5-oxo-, methyl ester

127452-95-3

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Basic information

Product Name: 3-Cyclohexene-1-carboxylic acid, 1-(2-bromoethyl)-3-methoxy-5-oxo-, methyl ester
Synonyms:
CAS NO:127452-95-3
Molecular Formula: C11H15BrO4
Molecular Weight: 291.142
EINECS: N/A
Product Categories: N/A
Mol File: 127452-95-3.mol

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: 3-Cyclohexene-1-carboxylic acid, 1-(2-bromoethyl)-3-methoxy-5-oxo-, methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-Cyclohexene-1-carboxylic acid, 1-(2-bromoethyl)-3-methoxy-5-oxo-, methyl ester(127452-95-3)
EPA Substance Registry System: 3-Cyclohexene-1-carboxylic acid, 1-(2-bromoethyl)-3-methoxy-5-oxo-, methyl ester(127452-95-3)

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: 127452-95-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 127452-95-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,4,5 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 127452-95:
(8*1)+(7*2)+(6*7)+(5*4)+(4*5)+(3*2)+(2*9)+(1*5)=133
133 % 10 = 3
So 127452-95-3 is a valid CAS Registry Number.

127452-95-3Upstream product

59741-89-8 methyl 1-(2-bromoethyl)-3,5-dimethoxycyclohexa-2,5-diene-1-carboxylate

127452-95-3Downstream Products

127452-95-3Relevant academic research and scientific papers

Preparation of Bicyclic Herbicide Precursors by Intramolecular Stork-Danheiser Kinetic Alkylation Reactions of Methyl 1-(Haloalkyl)-3-methoxy-5-oxocyclohex-3-ene-1-carboxylate Derivatives

Liepa, Andris J.,Wilkie, John S.,Winkler, David A.,Winzenberg, Kevin N.

, p. 759 - 767 (2007/10/02)

Reductive alkylation of methyl 3,5-dimethoxybenzoate with the dibromoalkane and the bromochloroalkane derivatives (4a-d) and (4e-g) afforded, after acid hydrolysis, the corresponding methyl 1-(haloalkyl)-3-methoxy-5-oxocyclohex-3-ene-1-carboxylate derivat

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