65355-36-4

Basic information

• Product Name: [trans(trans)]-4'-pentyl[1,1'-bicyclohexyl]-4-carbonitrile
• Synonyms: [trans(trans)]-4'-pentyl[1,1'-bicyclohexyl]-4-carbonitrile;(1,1'-Bicyclohexyl)-4-carbonitrile, 4'-pentyl-, (trans,trans)-;Einecs 265-713-3;trans-4-N-Pentyl-trans-dicyclohexyl-4'-carbonitrile
• CAS NO: 65355-36-4
• Molecular Formula: C₁₈H₃₁N
• Molecular Weight: 261.44544
• EINECS: 265-713-3
• Mol File: 65355-36-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 383.0±11.0 °C(Predicted)
• Appearance: /
• Density: 0.92±0.1 g/cm3(Predicted)
• CAS DataBase Reference: [trans(trans)]-4'-pentyl[1,1'-bicyclohexyl]-4-carbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: [trans(trans)]-4'-pentyl[1,1'-bicyclohexyl]-4-carbonitrile(65355-36-4)
• EPA Substance Registry System: [trans(trans)]-4'-pentyl[1,1'-bicyclohexyl]-4-carbonitrile(65355-36-4)

Safety Data

• Hazardous Substances Data: 65355-36-4(Hazardous Substances Data)

Usage

General Description

The chemical [trans(trans)]-4'-pentyl[1,1'-bicyclohexyl]-4-carbonitrile is a complex organic compound with a molecular formula C25H35N and a molecular weight of 341.55 g/mol. It belongs to the class of substituted benzonitrile compounds and is characterized by the presence of a pentyl group and a bicyclohexyl moiety. This chemical is often used in the field of organic synthesis and material science due to its versatile reactivity and interesting physical properties. Its unique structure and properties make it an important building block for the development of advanced materials and pharmaceuticals. Additionally, it has potential applications in the field of liquid crystals and organic electronics due to its intriguing molecular structure.

Upstream product

• 65355-30-8 4-(Trans-4'-pentylcyclohexyl)-benzoic acid 
• 65355-33-1 trans-4-cyclohexyl-1-carboxylic acid 

Downstream Products

• 65355-33-1 trans-4-cyclohexyl-1-carboxylic acid 
• 82598-08-1 4-n-pentyl-trans,trans-bicyclohexyl-4'-carbinol 

Relevant articles and documents

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

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.