70784-10-0 Usage
Uses
Used in Organic Synthesis:
[trans(trans)]-4'-butyl[1,1'-bicyclohexyl]-4-carbonitrile is used as a building block in organic synthesis for its unique structure and properties, allowing for the creation of a wide range of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [trans(trans)]-4'-butyl[1,1'-bicyclohexyl]-4-carbonitrile is used as an intermediate in the synthesis of various pharmaceuticals. Its unique structure and properties make it a valuable component in the development of new drugs.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, [trans(trans)]-4'-butyl[1,1'-bicyclohexyl]-4-carbonitrile is utilized as a building block for the preparation of different agrochemicals, contributing to the development of innovative products for agricultural applications.
Check Digit Verification of cas no
The CAS Registry Mumber 70784-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,7,8 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70784-10:
(7*7)+(6*0)+(5*7)+(4*8)+(3*4)+(2*1)+(1*0)=130
130 % 10 = 0
So 70784-10-0 is a valid CAS Registry Number.
70784-10-0Relevant 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.
