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AB55301

1131-09-5 | Benzo[b]thiophene-3-acetic acid

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $18.00 $13.00 -   +
1g 98% in stock $34.00 $24.00 -   +
5g 98% in stock $169.00 $119.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB55301
Chemical Name: Benzo[b]thiophene-3-acetic acid
CAS Number: 1131-09-5
Molecular Formula: C10H8O2S
Molecular Weight: 192.2343
MDL Number: MFCD00051637
SMILES: OC(=O)Cc1csc2c1cccc2

 

Computed Properties
Complexity: 205  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
XLogP3: 2.4  

 

 

Upstream Synthesis Route
  • (Benzo[b]thiophen-3-yl)acetic acid, also known as $name$, is a versatile compound widely utilized in chemical synthesis for various applications. One key use of (Benzo[b]thiophen-3-yl)acetic acid is as a building block for the synthesis of complex organic molecules and pharmaceuticals. Its unique chemical structure and reactivity make it an essential component in the creation of novel compounds with diverse properties.In organic synthesis, (Benzo[b]thiophen-3-yl)acetic acid serves as a valuable starting material for the preparation of heterocyclic compounds, which are commonly found in pharmaceuticals, agrochemicals, and materials science. Its aromatic ring and carboxylic acid functional group enable the introduction of various substituents and modifications, allowing for the fine-tuning of molecular properties.Additionally, (Benzo[b]thiophen-3-yl)acetic acid can participate in cross-coupling reactions, such as Suzuki-Miyaura and Heck coupling, to form biaryl compounds and functionalized products. These transformations expand the chemical diversity and complexity of the synthesized molecules, offering new possibilities for drug discovery and material development.Furthermore, (Benzo[b]thiophen-3-yl)acetic acid is employed in the construction of diverse scaffolds and intermediates, facilitating the rapid and efficient synthesis of target molecules in medicinal chemistry and chemical biology. Its versatility and compatibility with various reaction conditions make it a valuable tool for organic chemists seeking to access structurally diverse and biologically relevant compounds.Overall, (Benzo[b]thiophen-3-yl)acetic acid plays a crucial role in chemical synthesis by enabling the efficient assembly of complex molecules, driving innovation in drug discovery, materials science, and chemical research.
Literature
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