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2,2-dimethoxy-cyclohexanecarboxylic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

233262-34-5

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233262-34-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 233262-34-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,3,2,6 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 233262-34:
(8*2)+(7*3)+(6*3)+(5*2)+(4*6)+(3*2)+(2*3)+(1*4)=105
105 % 10 = 5
So 233262-34-5 is a valid CAS Registry Number.

233262-34-5SDS

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 methyl 2,2-dimethoxycyclohexanecarboxylate

1.2 Other means of identification

Product number -
Other names -

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:233262-34-5 SDS

233262-34-5Relevant academic research and scientific papers

Regiochemistry of the reaction of 2-acylcyclohexanones with trimethyl orthoformate: A convenient one-pot method to obtain 7,7-dimethoxy alkanoate methyl esters

Martins, Marcos A. P.,Bastos, Giovani P.,Sinhorin, Adilson P.,Flores, Alex F. C.,Bonacorso, Helio G.,Zanatta, Nilo

, p. 789 - 791 (1999)

The regiochemistry of the reaction of 2-acylcyclohexanones [containing 2-acyl groups, C(O)R, where R = Me, Et, CH2Ph, CF3, Ph and OMe] with trimethyl orthoformate to obtain the corresponding acetal derivative is reported. Compounds w

Diastereocontrol in the synthesis of models of rings C and D of phorbol: Directing effect of an ether substituent on lithium carbenoid mediated cyclopropanation

Drew, Michael G. B.,Harwood, Laurence M.,Macias-Sanchez, Antonio J.,Scott, Richard,Thomas,Uguen, Daniel

, p. 2311 - 2313 (2007/10/03)

The diastereocomplementarity of halo- and alkylcarbenes (paths a and b, respectively) was shown in the cyclopropanation reaction of 1. The conversion of 1 into 7,7-dimethylbicyclo[4.1.0]heptan-1,2-diols (±)-2 and (±)-3 represents an important transformati

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