21852-80-2 Usage
Description
1,9-Heptadecadiene-4,6-diyn-3-ol is a naturally occurring organic compound characterized by its unique structure, featuring a chain of 17 carbon atoms with triple bonds at the 4th and 6th positions and a hydroxyl group at the 3rd position. 1,9-Heptadecadiene-4,6-diyn-3-ol is derived from various plant sources and exhibits a range of biological activities, making it a potential candidate for pharmaceutical and industrial applications.
Uses
Used in Pharmaceutical Applications:
1,9-Heptadecadiene-4,6-diyn-3-ol is used as a bioactive compound for its potential therapeutic effects. It has been found to possess various pharmacological properties, such as anti-inflammatory, antioxidant, and anticancer activities. The compound's unique structure allows it to interact with specific biological targets, making it a promising candidate for the development of new drugs.
Used in Cosmetics Industry:
1,9-Heptadecadiene-4,6-diyn-3-ol is used as an active ingredient in the cosmetics industry for its potential skin benefits. The compound's antioxidant and anti-inflammatory properties may contribute to improved skin health and appearance, making it a valuable addition to skincare products.
Used in Agricultural Applications:
1,9-Heptadecadiene-4,6-diyn-3-ol is used as a natural pesticide or fungicide in the agricultural industry. Its bioactive properties may help protect crops from pests and diseases, promoting healthier plant growth and increased yield.
Used in Research and Development:
1,9-Heptadecadiene-4,6-diyn-3-ol is used as a research compound for studying its biological activities and potential applications in various fields. The compound's unique structure and properties make it an interesting subject for scientific investigation, which may lead to the discovery of new therapeutic agents or industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 21852-80-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,5 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21852-80:
(7*2)+(6*1)+(5*8)+(4*5)+(3*2)+(2*8)+(1*0)=102
102 % 10 = 2
So 21852-80-2 is a valid CAS Registry Number.
InChI:InChI=1/C17H24O/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17(18)4-2/h4,10-11,17-18H,2-3,5-9,12H2,1H3/b11-10-/t17-/m1/s1
21852-80-2Relevant articles and documents
A short synthesis of (+) and (-)-falcarinol
McLaughlin, Noel P.,Butler, Eibhlín,Evans, Paul,Brunton, Nigel P.,Koidis, Anastasios,Rai, Dilip K.
experimental part, p. 9681 - 9687 (2011/02/25)
A short, practical synthesis of the bis-acetylenic natural product falcarinol 1 is reported. This method relies on the alternate functionalisation of bis-trimethylsilylbutadiyne 10. This may be achieved in one-pot, however, better yields were obtained more conventionally. Lipase mediated enzymatic kinetic resolution of the racemic adduct in an organic solvent afforded (+)-1 in 97% enantiomeric excess. The analogous process performed with racemic 3-acetoxy falcarinol 11 under aqueous conditions gave (-)-1. Oxidation of 1 with Dess-Martin periodinane gave falcarinone 2.
Absolute configuration of falcarinol, a potent antitumor agent commonly occurring in plants
Zheng, Guangrong,Lu, Wei,Aisa, Haji A.,Cai, Junchao
, p. 2181 - 2182 (2007/10/03)
The absolute configuration of falcarinol (1) was established by stereoselective total synthesis of the two enantiomers.
