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65355-35-3

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65355-35-3 Usage

General Description

"[trans(trans)]-4'-propyl[1,1'-bicyclohexyl]-4-carbonitrile" is a chemical compound with a complex structure. It contains a propyl group and a carbonitrile group, both of which are connected to a bicyclohexyl ring system. The compound has a trans configuration, meaning that the substituent groups on the bicyclohexyl ring are on opposite sides of the molecule. [trans(trans)]-4'-propyl[1,1'-bicyclohexyl]-4-carbonitrile may have potential applications in various fields, including pharmaceuticals, materials science, and chemical synthesis. Its specific properties and potential uses would need to be further studied and evaluated.

Check Digit Verification of cas no

The CAS Registry Mumber 65355-35-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,5 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65355-35:
(7*6)+(6*5)+(5*3)+(4*5)+(3*5)+(2*3)+(1*5)=133
133 % 10 = 3
So 65355-35-3 is a valid CAS Registry Number.

65355-35-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-propylcyclohexyl)cyclohexane-1-carbonitrile

1.2 Other means of identification

Product number -
Other names trans,trans-4'-propyl-[1,1'-bicyclohexyl]-4-carbonitrile

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:65355-35-3 SDS

65355-35-3Relevant articles and documents

HYDROGENATION OF p-(trans-4-ALKYLCYCLOHEXYL) BENZOIC ACIDS IN ALKALINE CONDITIONS.

Karamysheva,Geivandova,Torgova,Kovshev,Betnev,Obukhova

, p. 1455 - 1459 (2007/10/02)

In a previous work it was shown that reduction of alkylbenzoic acids by sodium in amyl alcohol gives a higher percentage content of the trans isomer than other methods because of subsequent isomerization of the resultant mixture of cis and trans isomers of alkylcyclohexanecarboxylic acids under the influene of soidum alcoholate. In this work this method was used for reduction of p-(trans-4-alkylcyclohexyl)benzoic acids (II), the liquid-crystal properties of which are conclusive evidence of trans-1,4-diequatorial substitution of the cyclohexane group. Experimental evidence shows that reduction of p-(4-trans-butyclohexyl) benzoic acid (II) with Na/C//5H//1//1OH leads to formation of 4-trans-(4-trans-butylcyclohexyl) cyclohexaneacarboxylic left bracket (I)-trans right bracket and 4-cis-(4-trans-butylcyclohexyl) cyclohexanecarboxylic left bracket (I)-cis right bracket acids; in the course of reduction with NaOC//5H//1//1 the latter of these acids undergoes isomerization to (I)-trans to give an equilibrium mixture consisting of 92% (I)-trans and 8% (I)-cis.

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