77160-83-9 Usage
Uses
Used in Pharmaceutical Industry:
5-(N-(1'-phenylcyclohexyl)amino)pentanoic acid is used as a pharmaceutical compound for its potential therapeutic applications. The unique structure of this fatty acid derivative allows it to interact with specific biological targets, making it a promising candidate for the development of new drugs.
Used in Chemical Synthesis:
In the field of chemical synthesis, 5-(N-(1'-phenylcyclohexyl)amino)pentanoic acid serves as a key intermediate or building block for the creation of more complex molecules. Its unique functional groups and structural features enable the synthesis of a wide range of compounds with diverse applications.
Used in Material Science:
5-(N-(1'-phenylcyclohexyl)amino)pentanoic acid is used as a component in the development of novel materials with specific properties. Its incorporation into polymers or other materials can lead to enhanced performance characteristics, such as improved mechanical strength, thermal stability, or chemical resistance.
Used in Cosmetics Industry:
In the cosmetics industry, 5-(N-(1'-phenylcyclohexyl)amino)pentanoic acid may be utilized as an active ingredient in various formulations. Its unique properties could contribute to the development of innovative products with improved efficacy, such as anti-aging creams, skin care treatments, or hair care products.
Used in Research and Development:
5-(N-(1'-phenylcyclohexyl)amino)pentanoic acid is used as a research tool for studying the structure-activity relationships of fatty acid derivatives. Its unique structure allows scientists to explore the effects of different functional groups and substitutions on the compound's biological activity, potentially leading to the discovery of new therapeutic agents or materials with novel properties.
Check Digit Verification of cas no
The CAS Registry Mumber 77160-83-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,6 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 77160-83:
(7*7)+(6*7)+(5*1)+(4*6)+(3*0)+(2*8)+(1*3)=139
139 % 10 = 9
So 77160-83-9 is a valid CAS Registry Number.
InChI:InChI=1/C17H25NO2/c19-16(20)11-5-8-14-18-17(12-6-2-7-13-17)15-9-3-1-4-10-15/h1,3-4,9-10,18H,2,5-8,11-14H2,(H,19,20)
77160-83-9Relevant academic research and scientific papers
Metabolism of phencyclidine. The role of the carbinolamine intermediate in the formation of lactam and amino acid metabolites of nitrogen heterocycles
Baker,Little
, p. 46 - 50 (2007/10/02)
The transformation of phencyclidine in a mouse liver microsome preparation to several oxidative metabolites was studied. With use of GLC and HPLC methods with internal standards, phencyclidine and six metabolites were quantitated and the amino acid, resulting from the α-oxidation of the piperidine ring, was produced in 10-50 times greater amounts than the other metabolites. While most piperidines and pyrrolidines produce an amino acid and a corresponding lactam, it was found that phencyclidine was not converted to the lactam.
Mammalian metabolism of phencyclidine
Baker,Wohlford,Bradbury,Wirth
, p. 666 - 669 (2007/10/02)
In dogs, the major metabolite of phencyclidine was found to be 5-[N-(1'-phenylcyclohexyl) amino]pentanoic acid (1). The γ-aminobutyric acid like metabolite was also pharmacologically evaluated to determine if the purported GABA-ergic mediated effects of p
