1235-39-8 Usage
Description
(1S,8aα)-1,4aβ-Dimethyl-5β-(3-methyl-2,4-pentadienyl)-6-methylenedecalin-1β-carboxylic acid methyl ester is a complex organic compound characterized by its methyl ester derivative of a carboxylic acid, featuring multiple methyl and carboxylic acid functional groups. It possesses a bicyclic decalin ring structure and a distinctive side chain with a double bond and several methyl groups. This intricate chemical structure indicates potential applications in various fields, such as organic synthesis, pharmaceuticals, or as a flavor or fragrance ingredient. Further research and analysis are required to ascertain its specific properties and uses.
Uses
Used in Organic Synthesis:
(1S,8aα)-1,4aβ-Dimethyl-5β-(3-methyl-2,4-pentadienyl)-6-methylenedecalin-1β-carboxylic acid methyl ester is used as a key intermediate in organic synthesis for the development of novel compounds with potential applications in various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (1S,8aα)-1,4aβ-Dimethyl-5β-(3-methyl-2,4-pentadienyl)-6-methylenedecalin-1β-carboxylic acid methyl ester is utilized as a building block for the synthesis of new drug candidates, owing to its unique structural features and functional groups.
Used in Flavor and Fragrance Industry:
(1S,8aα)-1,4aβ-Dimethyl-5β-(3-methyl-2,4-pentadienyl)-6-methylenedecalin-1β-carboxylic acid methyl ester is employed as a component in the creation of unique fragrances and flavors, capitalizing on its complex chemical structure to produce distinct sensory properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1235-39-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,3 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1235-39:
(6*1)+(5*2)+(4*3)+(3*5)+(2*3)+(1*9)=58
58 % 10 = 8
So 1235-39-8 is a valid CAS Registry Number.
1235-39-8Relevant articles and documents
First enantiospecific syntheses of marine merosesquiterpenes neopetrosiquinones A and B: Evaluation of biological activity
Chayboun, Ikram,Boulifa, Ettahir,Mansour, Ahmed Ibn,Rodriguez-Serrano, Fernando,Carrasco, Esther,Alvarez, Pablo Juan,Chahboun, Rachid,Alvarez-Manzaneda, Enrique
, p. 1026 - 1036 (2015)
The first enantiospecific syntheses of neopetrosiquinones A (6) and B (7), two merosesquiterpenes isolated from the deep-water sponge Neopetrosia cf. proxima, from the labdane diterpene trans-communic acid (10) have been achieved. A key step of the synthetic sequence is the simultaneous aromatization of the C ring and the benzylic oxidation on C-7 of an advanced intermediate, mediated by the oxygen-DDQ system. The in vitro antiproliferative activities of neopetrosiquinone B (7) and of the synthetic intermediates 8 and 9 against human breast (MCF-7), lung (A-549), and colon (T-84) tumor cell lines have been assayed. The most potent was compound 9 (IC50 = 4.1 μM), which was twice as active as natural compound 7 (IC50 = 8.3 μM) against A-549 cells. In addition, the treatment with these compounds resulted in an induction of apoptosis. These findings indicate that the terpene benzoquinones reported here might be potentially useful as anticancer agents.
