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Atomfair (1-Benzothiophen-3-yl)boronic acid C8H7BO2S
Description (1-Benzothiophen-3-yl)boronic acid (CAS No. 113893-08-6) is a high-purity boronic acid derivative with the molecular formula C8H7BO2S . This compound is a valuable building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its stable boronic acid functional group. It features a benzothiophene core, making it useful for constructing heterocyclic compounds in pharmaceutical and materials science research. The product is supplied as a white to off-white crystalline powder with ??95% purity (HPLC), ensuring optimal performance in sensitive applications. Store in a cool, dry place under inert conditions to maintain stability.
Description
Description
(1-Benzothiophen-3-yl)boronic acid (CAS No. 113893-08-6) is a high-purity boronic acid derivative with the molecular formula C8H7BO2S. This compound is a valuable building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its stable boronic acid functional group. It features a benzothiophene core, making it useful for constructing heterocyclic compounds in pharmaceutical and materials science research. The product is supplied as a white to off-white crystalline powder with ??95% purity (HPLC), ensuring optimal performance in sensitive applications. Store in a cool, dry place under inert conditions to maintain stability.
- CAS No: 113893-08-6
- Molecular Formula: C8H7BO2S
- Molecular Weight: 178.02
- Exact Mass: 178.0259808
- Monoisotopic Mass: 178.0259808
- IUPAC Name: 1-benzothiophen-3-ylboronic acid
- SMILES: B(C1=CSC2=CC=CC=C12)(O)O
- Synonyms: (1-benzothiophen-3-yl)boronic acid, 808-005-7, 113893-08-6, Benzothiophene-3-boronic acid, 1-benzothiophen-3-ylboronic acid
Application
(1-Benzothiophen-3-yl)boronic acid is widely used in palladium-catalyzed cross-coupling reactions to synthesize biaryl and heteroaryl compounds. It serves as a key intermediate in the development of pharmaceuticals, agrochemicals, and organic electronic materials. Researchers also employ it in the synthesis of benzothiophene-based ligands for catalysis and sensor applications.
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