1279119-66-2 Usage
Description
Cyclopropaneundecanoic acid is a saturated fatty acid with a molecular formula C15H28O2, featuring a unique cyclopropane ring structure that contributes to its stability and resistance to oxidation. It is commonly found in plant oils such as coconut oil and Isatis tinctoria oil and has been explored for various pharmaceutical and industrial applications.
Uses
Used in Pharmaceutical Applications:
Cyclopropaneundecanoic acid is used as an antimicrobial and anti-inflammatory agent due to its demonstrated activity against antibiotic-resistant bacteria, making it a potential candidate for the development of new treatments for infectious diseases.
Used in Biofuel Production:
Cyclopropaneundecanoic acid is used as a renewable and sustainable energy source in biofuel production, offering an environmentally friendly alternative to traditional fossil fuels. Its potential use in this industry highlights its versatility and applicability in addressing energy and environmental concerns.
Check Digit Verification of cas no
The CAS Registry Mumber 1279119-66-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,9,1,1 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1279119-66:
(9*1)+(8*2)+(7*7)+(6*9)+(5*1)+(4*1)+(3*9)+(2*6)+(1*6)=182
182 % 10 = 2
So 1279119-66-2 is a valid CAS Registry Number.
1279119-66-2Relevant articles and documents
Stereoselective synthesis of a promising flower-inducing KODA analog, (9R,12S,13R,15Z)-9-hydroxy-12,13-methylene-10-oxooctadec-15-enoic acid
Shimomura, Shin,Oyama, Shuho,Nakano, Kyohei,Hasegawa, Morifumi,Toshima, Hiroaki
, p. 1354 - 1357 (2013/07/26)
Stereoselective synthesis of a promising flower-inducing 9,10-ketol octadecadienoic acid (KODA) analog, (9R,12S,13R,15Z)-9-hydroxy-12,13-methylene- 10-oxooctadec-15-enoic acid, was designed to obtain the desired stereoisomer via coupling between chiral sulfone and aldehyde segments. A known chiral cyclopropane derivative was converted to the sulfone segment via carbon-chain elongation and sulfonylation. Dec-9-en-1-ol was converted to the aldehyde segment, whose C-9 configuration was introduced by Sharpless asymmetric dihydroxylation. Coupling of the both segments and subsequent assembly gave the desired (9R,12S,13R,15Z)-analog. The (9S,12S,13R,15Z)-analog was also synthesized by using the enatiomeric aldehyde segment. This strategy made it possible to synthesize the remaining stereoisomeric analogs.
