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Cyclohexanecarbonyl chloride, 4-octyl-, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80022-86-2

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80022-86-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80022-86-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,0,2 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 80022-86:
(7*8)+(6*0)+(5*0)+(4*2)+(3*2)+(2*8)+(1*6)=92
92 % 10 = 2
So 80022-86-2 is a valid CAS Registry Number.

80022-86-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-octylcyclohexane-1-carbonyl chloride

1.2 Other means of identification

Product number -
Other names trans-4-n-octylcyclohexane-carboxylic acid chloride

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:80022-86-2 SDS

80022-86-2Relevant academic research and scientific papers

Optically active mesomorphic compound and liquid crystal composition containing same

-

, (2008/06/13)

An optically active mesomorphic compound represented by the formula: STR1 wherein R1 denotes an alkyl group having 1-16 carbon atoms; R2 denotes an alkyl group having 1-18 carbon atoms; C* is an asymmetric carbon atom; X is an oxygen

The Synthesis and Liquid Crystal Properties of Some Laterally Fluorinated trans-Cyclohexane-1-carboxylate and Benzoate Esters

Gray, G. W.,Hogg, C.,Lacey, D.

, p. 1 - 24 (2007/10/02)

A large number of laterally fluorinated 4-n-alkyl- and -alkoxy-phenyl 4'-n-alkyl- and -alkoxy-bezoates and 4-n-alkylphenyl trans-4'-n-alkyl- and -alkoxy-cyclohexane-1-carboxylates were synthesised.In these compounds, the lateral fluoro-substituent was situated in either the phenol or the carboxylic acid moiety of the molecules for the benzoate esters, but only in the phenol moiety for the trans-cyclohexane-1-carboxylate esters.The nematic thermal stabilities for the fluorophenyl bezoate and trans-cyclohexane-1-carboxylate esters and the fluorobenzoate esters were compared with those for the corresponding non-fluorinated analogues.A nematic thermal efficiency order was derived for the 4-n-alkyl-fluorophenyl 4-n-alkylbezoate and trans-4-n-alkylcyclohexane-1-carboxylate esters, but only in the case of the latter esters, which were extensively examined, was the smectic tendency of the system investigated.Explanations are given for the observed nematic and smectic thermal stabilities of the titled esters, and some of their physical properties are discussed.

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