135569-29-8 Usage
Description
1-(4-Cyanophenyl)cyclopentanecarboxylic acid, also known as CPCC, is a chemical compound characterized by its molecular formula C13H11NO2. It features a carboxylic acid structure with a cyclopentane ring and a cyanophenyl group, making it a versatile building block in the synthesis of pharmaceutical and agrochemical products. As a white crystalline solid with a melting point of approximately 134-136 degrees Celsius, CPCC is sparingly soluble in water and should be handled with care due to potential health and environmental risks.
Uses
Used in Pharmaceutical Industry:
1-(4-Cyanophenyl)cyclopentanecarboxylic acid is used as a building block for the synthesis of various pharmaceutical products due to its versatile synthetic applications, contributing to the development of new medications and therapies.
Used in Agrochemical Industry:
1-(4-Cyanophenyl)cyclopentanecarboxylic acid is used as a starting material in the production of other organic compounds, particularly in the agrochemical sector, where it plays a role in the creation of substances for pest control and crop protection.
Used in Organic Chemistry:
1-(4-Cyanophenyl)cyclopentanecarboxylic acid is used as a key intermediate in organic chemistry for the synthesis of a wide range of compounds, showcasing its utility in various chemical reactions and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 135569-29-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,5,6 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 135569-29:
(8*1)+(7*3)+(6*5)+(5*5)+(4*6)+(3*9)+(2*2)+(1*9)=148
148 % 10 = 8
So 135569-29-8 is a valid CAS Registry Number.
135569-29-8Relevant articles and documents
Muscarinic Receptor Binding Profile of Para-Substituted Caramiphen Analogues
Hudkins, Robert L.,DeHaven-Hudkins, Diane L.,Stubbins, James F.
, p. 2984 - 2989 (2007/10/02)
Para-substituted analogues of the antimuscarinic agent caramiphen were synthesized and evaluated for their ability to bind to the M1 and M2 subtypes of the muscarinic receptor.The purpose of the set to look for a possible relationshi
