29780-00-5 Usage
Uses
Used in Skincare Products:
DELTA 12 CIS TRIDECENOIC ACID METHYL ESTER is used as an active ingredient in skincare products for its potential moisturizing and anti-inflammatory properties, which can help improve skin health and appearance.
Used in Pharmaceutical Industry:
DELTA 12 CIS TRIDECENOIC ACID METHYL ESTER is used as a pharmaceutical compound for its potential therapeutic effects in the prevention and treatment of various diseases and conditions, such as inflammation, cancer, and neurological disorders.
Used as a Flavoring Agent in the Food Industry:
DELTA 12 CIS TRIDECENOIC ACID METHYL ESTER is used as a flavoring agent in the food industry, adding unique taste and aroma profiles to various food products.
Overall, DELTA 12 CIS TRIDECENOIC ACID METHYL ESTER is a multifaceted compound with a broad spectrum of potential applications across different industries, including skincare, pharmaceuticals, and food, due to its unique chemical structure and therapeutic properties.
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 academic research and scientific papers
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.
