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67589-92-8

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67589-92-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67589-92-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,8 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 67589-92:
(7*6)+(6*7)+(5*5)+(4*8)+(3*9)+(2*9)+(1*2)=188
188 % 10 = 8
So 67589-92-8 is a valid CAS Registry Number.

67589-92-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-heptylcyclohexane-1-carbonyl chloride

1.2 Other means of identification

Product number -
Other names Cyclohexanecarbonyl chloride,4-heptyl-,trans

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:67589-92-8 SDS

67589-92-8Relevant articles and documents

Synthesis and Physical Properties of Alkoxymethylene Substituted Phenyl Cyclohexanecarboxylates

Kitamura, Teruo,Mukoh, Akio,Era, Susumu,Fujii, Tsunenori

, p. 231 - 248 (2007/10/02)

The homologous series of 4-alkoxymethylene-substituted-phenyl 4'-alkylcyclohexanecarboxylates are prepared.And their transition temperatures, bulk viscosities and birefringences have been measured comparing with the series of 4-alkoxy-substituted-phenyl 4'-alkylcyclohexanecarboxylates.The differences between the alkoxymethylene-substituted series and alkoxy-substituted series are discussed.Alkoxymethylene groups contribute to lowering the transition temperatures, and also reducing the bulk viscosities and optical anisotropy compared to the alkoxy groups as terminal groups of mesogens.This is apparently due to the higher flexibility of the alkoxymethylene groups, which affected the packing of molecules.

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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