3260-92-2 Usage
Description
1-(3-hydroxybenzo[b]thien-2-yl)-Ethanon, also known as 3-Hydroxy-1-(benzo[b]thiophen-2-yl)ethanone, is a chemical compound characterized by its molecular formula C12H10O2S. This ketone derivative features a benzo[b]thiophene ring and a hydroxy functional group, making it a versatile building block in organic synthesis and pharmaceutical research. With a molecular weight of 218.27 g/mol and a melting point of 150-152°C, it is typically found as a yellow powder. Its unique structure and properties have garnered interest in the field of medicinal and pharmaceutical chemistry, particularly for its potential anti-inflammatory and anticancer properties.
Uses
Used in Pharmaceutical Research:
1-(3-hydroxybenzo[b]thien-2-yl)-Ethanon is utilized as a key building block in the synthesis of various bioactive molecules, contributing to the development of new pharmaceuticals. Its chemical structure allows for the creation of compounds with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(3-hydroxybenzo[b]thien-2-yl)-Ethanon serves as an important intermediate for the production of a wide range of chemical compounds. Its versatility in forming different molecular structures makes it a valuable asset in the synthesis of complex organic molecules.
Used in Anti-inflammatory Applications:
1-(3-hydroxybenzo[b]thien-2-yl)-Ethanon has been studied for its potential anti-inflammatory properties, which could make it a useful compound in the development of treatments for various inflammatory conditions.
Used in Anticancer Applications:
1-(3-hydroxybenzo[b]thien-2-yl)-Ethanon has also been investigated for its potential anticancer properties, with research focusing on its ability to target and inhibit cancer cell growth. If successful, it could be integrated into the development of novel cancer therapies.
Used in Medicinal Chemistry:
1-(3-hydroxybenzo[b]thien-2-yl)-Ethanon's unique structure and properties make it a valuable addition to the field of medicinal chemistry, where it can be used to design and develop new drugs with improved efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 3260-92-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,6 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3260-92:
(6*3)+(5*2)+(4*6)+(3*0)+(2*9)+(1*2)=72
72 % 10 = 2
So 3260-92-2 is a valid CAS Registry Number.
3260-92-2Relevant articles and documents
Action de reactifs nucleophiles sur les phenyl-5 thienopyrannone-7 et phenyl-2 benzothienoprannone-4
Netchitailo, Pierre,Decroix, Bernard,Morel, Jean
, p. 327 - 333 (2007/10/02)
Reactions of 5-phenylthienopyran-7-one, 2-phenylbenzothienopyran-4-one and the corresponding thiones with sodium ethylate, guanidines, hydrazines and amines are describred and compared to those observed with benzopyranones.