97023-48-8 Usage
Description
2-Cyclohexylbenzoic Acid is an organic compound characterized by a cyclohexane ring attached to a benzene ring, with a carboxylic acid group. It possesses unique chemical properties that make it a versatile reagent in various chemical processes.
Uses
Used in Organic Synthesis:
2-Cyclohexylbenzoic Acid is used as a reagent in organic synthesis for the preparation of various chemical compounds. Its unique structure allows it to participate in a range of reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Chemical Processes:
2-Cyclohexylbenzoic Acid is also utilized in various chemical processes, such as catalysis and polymerization. Its ability to interact with other molecules and participate in different types of reactions makes it a useful intermediate in the production of a wide range of chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 97023-48-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,0,2 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 97023-48:
(7*9)+(6*7)+(5*0)+(4*2)+(3*3)+(2*4)+(1*8)=138
138 % 10 = 8
So 97023-48-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H16O2/c14-13(15)12-9-5-4-8-11(12)10-6-2-1-3-7-10/h4-5,8-10H,1-3,6-7H2,(H,14,15)
97023-48-8Relevant articles and documents
Strategic Approach to the Metamorphosis of γ-Lactones to NH γ-Lactams via Reductive Cleavage and C-H Amidation
Jung, Hoi-Yun,Chang, Sukbok,Hong, Sungwoo
supporting information, p. 7099 - 7103 (2019/09/07)
A new approach has elaborated on the conversion of γ-lactones to the corresponding NH γ-lactams that can serve as γ-lactone bioisosteres. This approach consists of reductive C-O cleavage and an Ir-catalyzed C-H amidation, offering a powerful synthetic tool for accessing a wide range of valuable NH γ-lactam building blocks starting from γ-lactones. The synthetic utility was further demonstrated by the late-stage transformation of complex bioactive molecules and the asymmetric transformation.
Pincer thioamide and pincer thioimide palladium complexes catalyze highly efficient negishi coupling of primary and secondary alkyl zinc reagents at room temperature
Wang, Haibo,Liu, Jing,Deng, Yi,Min, Tianyin,Yu, Ganxiang,Wu, Xiaojun,Yang, Zhen,Lei, Aiwen
supporting information; experimental part, p. 1499 - 1507 (2009/08/07)
Pincer thioamide PdII complex 2 was prepared, and its reaction with cyclohexylzinc chloride yielded novel pincer thioimide PdII complex 3 besides Pd0 species. The structures of complexes 2 and 3 were confirmed by X-ray ana
