60263-54-9 Usage
Description
[1,1'-bicyclohexyl]-1-carboxylic acid, also known as bicyclohexylcarboxylic acid, is a cyclohexanecarboxylic acid derivative in which the hydrogen attached to the alpha-carbon is substituted by a cyclohexyl group. This organic compound possesses unique structural properties that contribute to its various applications across different industries.
Uses
Used in Pharmaceutical Industry:
[1,1'-bicyclohexyl]-1-carboxylic acid is used as an active pharmaceutical ingredient for its antispasmodic power. It helps in alleviating muscle spasms and cramps, providing relief to patients suffering from various conditions that cause involuntary muscle contractions.
Used in Chemical Synthesis:
In the chemical industry, [1,1'-bicyclohexyl]-1-carboxylic acid serves as a key intermediate in the synthesis of various organic compounds and pharmaceuticals. Its unique bicyclic structure allows for the creation of a wide range of derivatives with diverse applications.
Used in Research and Development:
Due to its unique structural properties, [1,1'-bicyclohexyl]-1-carboxylic acid is utilized in research and development for the study of organic chemistry, drug discovery, and the development of new materials with specific properties.
Check Digit Verification of cas no
The CAS Registry Mumber 60263-54-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,2,6 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60263-54:
(7*6)+(6*0)+(5*2)+(4*6)+(3*3)+(2*5)+(1*4)=99
99 % 10 = 9
So 60263-54-9 is a valid CAS Registry Number.
60263-54-9Relevant articles and documents
Studies in Alicyclic Compounds: Part VII - Koch-Haaf Carboxylation of 1-Cycloalkylcycloalkanols
Rao, R. R.,Bhattacharya, S.
, p. 207 - 209 (2007/10/02)
The Koch-Haaf carboxylation (K-H-C) of 1-cycloalkylcyclopentanols (Ia and Ib) and 1-cycloalkylcyclohexanols (VIa and VIb) has been investigated.In the case of 1-cycloalkylcyclopentanols (Ia and Ib), K-H-C results in the formation of rearranged tertiary (30) bridgehead acids (Va and Vb) providing interesting examples of ring expansion reactions, whereas K-H-C of 1-cycloalkylcyclohexanols (VIa and VIb) furnishes the corresponding 30 carboxylic acids (VIIIa and VIIIb) in good yields.
