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3-Cyclohexene-1-carboxylic acid, 1-methyl-6-oxo-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

134906-27-7

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134906-27-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134906-27-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,9,0 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 134906-27:
(8*1)+(7*3)+(6*4)+(5*9)+(4*0)+(3*6)+(2*2)+(1*7)=127
127 % 10 = 7
So 134906-27-7 is a valid CAS Registry Number.

134906-27-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1-methyl-6-oxocyclohex-3-ene-1-carboxylate

1.2 Other means of identification

Product number -
Other names 3-Cyclohexene-1-carboxylic acid,1-methyl-6-oxo-,ethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:134906-27-7 SDS

134906-27-7Downstream Products

134906-27-7Relevant academic research and scientific papers

Reaction of enol ethers with alkynes catalyzed by transition metals: 5-exo-dig versus 6-endo-dig cyclizations via cyclopropyl platinum or gold carbene complexes

Nevado, Cristina,Cardenas, Diego J.,Echavarren, Antonio M.

, p. 2627 - 2635 (2003)

The intramolecular reaction of enol ethers with alkynes in methanol is catalyzed by electrophilic PtII, PdII, and AuIII chlorides and by a Cu1 complex to give five- or six-membered rings bearing dimethyl acetals

Solvent Effects on Manganese(III)-Based Oxidative Free-Radical Cyclizations: Ethanol and Acetic Acid

Snider, Barry B.,Merritt, John E.,Dombroski, Mark A.,Buckman, Brad O.

, p. 5544 - 5553 (2007/10/02)

Ethanol complements the typical solvent, acetic acid, for Mn(III)-based oxidative free-radical cyclizations.Cyclization of enol ether 1c to give gibberellic acid intermediate 6c is successfull in ethanol, but not in acetic acid.Ethanol acts as a reducing

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