69727-30-6 Usage
Description
(10Z)-12-oxooctadec-10-enoic acid is a long-chain fatty acid belonging to the class of organic compounds. It is a carboxylic acid with an 18-carbon chain and a double bond at the 10th position. (10Z)-12-oxooctadec-10-enoic acid is commonly found in natural sources and plays a significant role in various biological processes, including lipid synthesis, production of signaling molecules, and cellular communication and inflammation. It also has potential therapeutic applications in dermatology and immunology.
Uses
Used in Pharmaceutical Industry:
(10Z)-12-oxooctadec-10-enoic acid is used as a precursor for the production of signaling molecules, which are essential for cellular communication and inflammation. Its role in these processes makes it a valuable compound for the development of pharmaceuticals targeting inflammation and related conditions.
Used in Dermatology:
(10Z)-12-oxooctadec-10-enoic acid is used as an active ingredient in dermatological applications due to its potential therapeutic effects on skin health and conditions. Its involvement in lipid synthesis and cellular communication may contribute to its beneficial properties for skin care and treatment of skin disorders.
Used in Immunology:
(10Z)-12-oxooctadec-10-enoic acid is used as a research compound in immunology to study its potential effects on the immune system. Its role in cellular communication and inflammation suggests that it may have applications in modulating immune responses and treating immune-related conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 69727-30-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,2 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 69727-30:
(7*6)+(6*9)+(5*7)+(4*2)+(3*7)+(2*3)+(1*0)=166
166 % 10 = 6
So 69727-30-6 is a valid CAS Registry Number.
69727-30-6Relevant articles and documents
Stereochemistry of Olefin and Fatty Acid Oxidation. Part 3. The Allylic Hydroperoxides from the Autoxidation of Methyl Oleate
Frankel, Edwin N.,Garwood, Robert F.,Khambay, Bhupinder P. S.,Moss, Gerard P.,Weedon, Basil C. L.
, p. 2233 - 2240 (2007/10/02)
Methods have been developed, using 13C n.m.r. spectroscopy and mass spectrometry, for the analysis of all eight cis and trans allylic 8-, 9-, 10-, and 11-hydroperoxides formed on autoxidation of methyl oleate.
