1279119-66-2 Usage
General Description
Cyclopropaneundecanoic acid is a chemical compound with a molecular formula C15H28O2. It is a saturated fatty acid with a unique cyclopropane ring structure, making it relatively stable and resistant to oxidation. It is commonly found in certain plant oils, such as coconut oil and Isatis tinctoria oil, and has been investigated for potential pharmaceutical and industrial applications. Cyclopropaneundecanoic acid exhibits antimicrobial and anti-inflammatory properties, and has shown promising activity against antibiotic-resistant bacteria. Additionally, it has been studied for its potential use in biofuel production as a renewable and sustainable energy source.
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.
