65355-36-4 Usage
Uses
Used in Organic Synthesis:
[trans(trans)]-4'-pentyl[1,1'-bicyclohexyl]-4-carbonitrile is used as a building block for the synthesis of various organic compounds due to its versatile reactivity and interesting physical properties.
Used in Material Science:
[trans(trans)]-4'-pentyl[1,1'-bicyclohexyl]-4-carbonitrile is used as a component in the development of advanced materials due to its unique structure and properties.
Used in Pharmaceutical Industry:
[trans(trans)]-4'-pentyl[1,1'-bicyclohexyl]-4-carbonitrile is used as a building block for the development of pharmaceuticals due to its unique structure and properties.
Used in Liquid Crystals:
[trans(trans)]-4'-pentyl[1,1'-bicyclohexyl]-4-carbonitrile is used as a component in the development of liquid crystals due to its intriguing molecular structure.
Used in Organic Electronics:
[trans(trans)]-4'-pentyl[1,1'-bicyclohexyl]-4-carbonitrile is used as a component in the development of organic electronics due to its intriguing molecular structure.
Check Digit Verification of cas no
The CAS Registry Mumber 65355-36-4 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 65355-36:
(7*6)+(6*5)+(5*3)+(4*5)+(3*5)+(2*3)+(1*6)=134
134 % 10 = 4
So 65355-36-4 is a valid CAS Registry Number.
65355-36-4Relevant academic research and scientific papers
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.
