131647-21-7 Usage
Description
(4aS,8aS)-octahydro-3H-isochromen-3-one, also known as dihydroisocoumarin, is a chemical compound with the molecular formula C9H14O2. It is a cyclic enol ether and a lactone, commonly found in natural products such as coumarins and flavonoids. (4aS,8aS)-octahydro-3H-isochromen-3-one features a unique six-membered ring structure, making it an important intermediate for the synthesis of various heterocyclic compounds. It is also recognized for its potential biological activities, including antimicrobial, antioxidant, and anti-inflammatory properties, which position it as a target for research in drug discovery and development.
Uses
Used in Pharmaceutical Industry:
(4aS,8aS)-octahydro-3H-isochromen-3-one is used as an intermediate for the synthesis of various heterocyclic compounds, which are essential in the development of new medicines. Its unique ring structure and biological activities contribute to its significance in the pharmaceutical sector.
Used in Fragrance Industry:
In the fragrance industry, (4aS,8aS)-octahydro-3H-isochromen-3-one is used as a building block for the production of perfumes. Its presence in natural products like coumarins and flavonoids makes it a valuable component in creating complex and appealing scents.
Used in Drug Discovery and Development:
(4aS,8aS)-octahydro-3H-isochromen-3-one is used as a target for research in drug discovery and development due to its potential antimicrobial, antioxidant, and anti-inflammatory properties. These characteristics make it a promising candidate for the creation of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 131647-21-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,6,4 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 131647-21:
(8*1)+(7*3)+(6*1)+(5*6)+(4*4)+(3*7)+(2*2)+(1*1)=107
107 % 10 = 7
So 131647-21-7 is a valid CAS Registry Number.
131647-21-7Relevant articles and documents
A new strategy for the synthesis of himbacine
Casey, Mike,McCarthy, Robert
, p. 801 - 804 (2011/06/11)
A new strategy for the assembly of himbacine and analogues, which display potent biological activity, is described. A four-step route to a key intermediate has been developed, in which the key step is a highly diastereoselective Michael-Dieckmann domino reaction. Use of an enantioenriched Michael acceptor, readily obtained by an asymmetric dihydroxylation reaction, allowed kinetic resolution of the Michael donor, which was itself prepared by a domino reaction. Georg Thieme Verlag Stuttgart.
