AB55301
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.
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 |
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 |
(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.
Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501