1380792-92-6 Usage
Description
(S)-2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid is a chiral chemical compound derived from benzofuran, a heterocyclic compound featuring a fused benzene and furan ring. As a chiral molecule, it possesses an asymmetrical carbon atom, which grants it optical activity. (S)-2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid comprises a carboxylic acid group and a hydroxyl substituent, with the benzofuran ring having a hydroxyl group at the 6-position. The unique structure and functional groups of (S)-2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid may endow it with potential pharmaceutical or biological applications.
Uses
Used in Pharmaceutical Applications:
(S)-2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid is used as a pharmaceutical compound for its potential therapeutic properties. The presence of a carboxylic acid group and a hydroxyl substituent allows for interactions with various biological targets, which could be harnessed for the development of new drugs.
Used in Chemical Synthesis:
In the chemical industry, (S)-2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid can be used as a building block or intermediate in the synthesis of more complex molecules. Its unique structure and functional groups make it a valuable component in the creation of novel chemical entities with specific applications.
Used in Research and Development:
(S)-2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid serves as a valuable compound in research and development, particularly in the fields of organic chemistry and medicinal chemistry. Its unique structure and optical activity make it an interesting subject for studying the effects of chirality on biological activity and the development of enantioselective synthetic methods.
Used in Drug Delivery Systems:
Similar to gallotannin, (S)-2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid could potentially be employed in drug delivery systems. Its functional groups may allow for the development of novel carriers or enhancers for drug molecules, improving their delivery, bioavailability, and therapeutic outcomes.
Check Digit Verification of cas no
The CAS Registry Mumber 1380792-92-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,7,9 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1380792-92:
(9*1)+(8*3)+(7*8)+(6*0)+(5*7)+(4*9)+(3*2)+(2*9)+(1*2)=186
186 % 10 = 6
So 1380792-92-6 is a valid CAS Registry Number.
1380792-92-6Relevant articles and documents
FUSED HETEROCYCLIC COMPOUND
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, (2015/09/22)
A fused heterocyclic compound having an enteropeptidase inhibitory action and use of the compound as a medicament for treatment or prophylaxis of obesity, diabetes mellitus, etc., are provided. Specifically, a compound represented by the following formula (I): wherein each symbol is as defined herein, or a salt thereof and use of the compound as a medicament for treatment or prophylaxis of obesity, diabetes mellitus, etc., are provided.
PRODUCTION METHOD OF OPTICALLY ACTIVE DIHYDROBENZOFURAN DERIVATIVE
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Page/Page column 176, (2012/09/10)
Provided is a production method of an optically active dihydrobenzofuran derivative. A production method of an optically active form of a compound represented by the formula: wherein each symbol is as defined in the specification, or a salt thereof and the like.
