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Atomfair Benzo[b]naphtho[1,2-d]thiophen-5-ylboronic acid C16H11BO2S

Description Benzo[b]naphtho[1,2-d]thiophen-5-ylboronic acid (CAS No. 1447709-01-4) is a high-purity boronic acid derivative with the molecular formula C16H11BO2S . This compound features a polycyclic aromatic structure fused with a thiophene ring, making it a valuable intermediate in organic synthesis and materials science. Its IUPAC name, naphtho[2,1-b][1]benzothiol-5-ylboronic acid , reflects its complex heterocyclic architecture. Ideal for Suzuki-Miyaura cross-coupling reactions, this boronic acid is rigorously tested for quality, ensuring optimal reactivity and yield. Suitable for researchers in pharmaceuticals, OLED development, and advanced material design, it is available in various quantities with detailed analytical data (NMR, HPLC, MS) upon request. Store under inert conditions…

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Description

Description

Benzo[b]naphtho[1,2-d]thiophen-5-ylboronic acid (CAS No. 1447709-01-4) is a high-purity boronic acid derivative with the molecular formula C16H11BO2S. This compound features a polycyclic aromatic structure fused with a thiophene ring, making it a valuable intermediate in organic synthesis and materials science. Its IUPAC name, naphtho[2,1-b][1]benzothiol-5-ylboronic acid, reflects its complex heterocyclic architecture. Ideal for Suzuki-Miyaura cross-coupling reactions, this boronic acid is rigorously tested for quality, ensuring optimal reactivity and yield. Suitable for researchers in pharmaceuticals, OLED development, and advanced material design, it is available in various quantities with detailed analytical data (NMR, HPLC, MS) upon request. Store under inert conditions to maintain stability.

  • CAS No: 1447709-01-4
  • Molecular Formula: C16H11BO2S
  • Molecular Weight: 278.1
  • Exact Mass: 278.0572809
  • Monoisotopic Mass: 278.0572809
  • IUPAC Name: naphtho[2,1-b][1]benzothiol-5-ylboronic acid
  • SMILES: B(C1=CC2=C(C3=CC=CC=C13)C4=CC=CC=C4S2)(O)O
  • Synonyms: 1447709-01-4, Benzo[b]naphtho[1,2-d]thiophen-5-ylboronic acid, Boronic acid, B-benzo[b]naphtho[1,2-d]thien-5-yl-, Benzo[b]naphtho[1,2-d]thien-5-ylboronic acid, naphtho[2,1-b][1]benzothiol-5-ylboronic acid

Application

Benzo[b]naphtho[1,2-d]thiophen-5-ylboronic acid is widely used as a key building block in Suzuki-Miyaura cross-coupling reactions to synthesize conjugated polymers and small molecules for organic electronics. Its rigid polycyclic structure makes it valuable in the development of high-performance OLED materials and organic semiconductors. Researchers also employ it in pharmaceutical intermediates for drug discovery targeting aromatic heterocycles. The compound’s boronic acid group enables efficient functionalization in catalytic cycles.

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