29780-00-5 Usage
General Description
Delta 12 cis tridecenoic acid methyl ester, also known as 12-tetradecenoic acid methyl ester, is a chemical compound consisting of a 12-carbon chain with a cis double bond at the 12th carbon and a methyl ester functional group. It is a commonly used fatty acid derivative in various industrial and pharmaceutical applications. DELTA 12 CIS TRIDECENOIC ACID METHYL ESTER is known for its potential therapeutic properties and is used in the production of skincare products, pharmaceuticals, and as a flavoring agent in the food industry. It is also being studied for its potential role in the prevention and treatment of various diseases and conditions, such as inflammation, cancer, and neurological disorders. Overall, delta 12 cis tridecenoic acid methyl ester is a versatile compound with a wide range of potential applications in different industries and therapeutic uses.
Check Digit Verification of cas no
The CAS Registry Mumber 29780-00-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,7,8 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 29780-00:
(7*2)+(6*9)+(5*7)+(4*8)+(3*0)+(2*0)+(1*0)=135
135 % 10 = 5
So 29780-00-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H26O2/c1-3-4-5-6-7-8-9-10-11-12-13-14(15)16-2/h3H,1,4-13H2,2H3
29780-00-5Relevant articles and documents
Synthesis of [14,14,14-2H3] 12-hydroxytetradecanoic acid and [13,14-2H2] 11-hydroxytetradecanoic acid useful as tracers to study a (11E)-desaturation reaction in Spodoptera littoralis
Navarro,Fabrias,Camps
, p. 439 - 443 (2007/10/03)
The synthesis of deuterium labeled 11- and 12-hydroxytetradecanoic acids to study a (11E) desaturase in the moth Spodoptera littoralis is reported. [14,14,14-2H3] 12-hydroxytetradecanoic acid was synthesized in four steps from 11-iodo-1-undecene in 49% overall yield. Deuterium was introduced by reaction of an epoxy ester with (CD3)2CuLi. The preparation of [13,14-2H2] 11-hydroxytetradecanoic acid was carried out in six steps from 11-bromoundecanoic acid in 55% overall yield. In this case, label was introduced by deuteration of an homoallyl alcohol with D2, using the Wilkinson catalyst. Incubation of pheromone glands with either of both acids did not lead to the formation of the labeled (11E)-tetradecanoic acid.
