7548-13-2 Usage
Description
Farnesoic acid is a methyl-branched, trienoic fatty acid, specifically dodeca-2,6,10-trienoic acid, which features three methyl substituents at the 3-, 7-, and 11-positions.
Uses
Used in Pharmaceutical Industry:
Farnesoic acid is used as a pharmaceutical agent for its potential role in modulating various biological processes. Its unique structure allows it to interact with specific targets and pathways, making it a candidate for the development of new drugs.
Used in Biochemical Research:
In the field of biochemical research, farnesoic acid is utilized as a tool compound to study the effects of methyl-branched fatty acids on cellular functions and signaling mechanisms. This can help researchers understand the role of these compounds in health and disease.
Used in Insect Hormone Research:
Farnesoic acid is also used in insect hormone research as it is a juvenile hormone analog. It can be employed to investigate the role of juvenile hormones in insect development, reproduction, and behavior, which can have implications for pest control strategies.
Used in Skin Care Industry:
In the skin care industry, farnesoic acid may be used as an ingredient in cosmetic products due to its potential benefits for skin health. Its effects on cellular processes could contribute to improved skin appearance and function.
Check Digit Verification of cas no
The CAS Registry Mumber 7548-13-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,4 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7548-13:
(6*7)+(5*5)+(4*4)+(3*8)+(2*1)+(1*3)=112
112 % 10 = 2
So 7548-13-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H24O2/c1-12(2)7-5-8-13(3)9-6-10-14(4)11-15(16)17/h7,9,11H,5-6,8,10H2,1-4H3,(H,16,17)/b13-9+,14-11+
7548-13-2Relevant articles and documents
Electrochemical Oxidation of Primary Alcohols to Aldehydes at the Nickel Hydroxide Electrode
Schneider, Roy,Schaefer, Hans-J.
, p. 742 - 743 (2007/10/02)
Primary alcohols were oxidized to aldehydes at the nickel hydroxide electrode in an emulsion of water and a nonpolar organic solvent.Benzylic and allylic primary alcohols afforded good yields, whereas the oxidation of saturated primary alcohols was less satisfactory.
