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3-methylphenyl cyclohexanecarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18731-59-4

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18731-59-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18731-59-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,3 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18731-59:
(7*1)+(6*8)+(5*7)+(4*3)+(3*1)+(2*5)+(1*9)=124
124 % 10 = 4
So 18731-59-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H18O2/c1-11-6-5-9-13(10-11)16-14(15)12-7-3-2-4-8-12/h5-6,9-10,12H,2-4,7-8H2,1H3

18731-59-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-methylphenyl) cyclohexanecarboxylate

1.2 Other means of identification

Product number -
Other names 3-Methylphenyl cyclohexanecarboxylate

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:18731-59-4 SDS

18731-59-4Relevant academic research and scientific papers

Influence of components of the PdCl2(PPh3) 2-PPh3-p-toluenesulfonic acid catalytic system on the rate of cyclohexene hydrocarbalkoxylation with m-cresol

Aver'yanov,Nosova,Astashina,Sevost'yanova

, p. 167 - 175 (2007)

Kinetic parameters were determined for the cyclohexene hydrocarbalkoxylation reaction catalyzed by the PdCl2(PPh 3)2-PPh3-p-toluenesulfonic acid (TSA) catalyst system in the presence of m-cresol. It was shown that the reaction is first order in cyclohexene and a fractional order in PdCl2(PPh 3)2 and m-cresol and that the dependences of the reaction rate on PCO, TSA and PPh3 concentrations are nonmonotonic in character. The inhibitory effect of tosylate and chloride ions on the reaction was revealed. The results were rationalized in terms of a mechanism that involves hydride complexes of the cation type as intermediates. A rate equation for the reaction was derived in terms of the steady-state hypothesis to fit to experimental data. Nauka/Interperiodica 2007.

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