Description
(4-Bromothieno[2,3-c]pyridin-2-yl)methanol (CAS No. 870243-94-0) is a high-purity heterocyclic compound featuring a brominated thienopyridine core with a hydroxymethyl functional group. This specialized chemical is designed for advanced research applications, particularly in pharmaceutical development, material science, and organic synthesis. With a molecular formula of C8H6BrNOS and a molecular weight of 244.11 g/mol, it offers exceptional reactivity for coupling reactions, functionalization, and as a building block for complex molecular architectures. The compound is supplied as a crystalline solid with ≥95% purity (HPLC), ensuring consistency in experimental results. Store under inert conditions at 2-8°C to maintain stability. Suitable for use in NMR, HPLC, and LC-MS analysis.
Properties
- CAS Number: 870243-94-0
- Complexity: 169
- IUPAC Name: (4-bromothieno[2,3-c]pyridin-2-yl)methanol
- InChI: InChI=1S/C8H6BrNOS/c9-7-2-10-3-8-6(7)1-5(4-11)12-8/h1-3,11H,4H2
- InChI Key: KDASDVVLOLIUDT-UHFFFAOYSA-N
- Exact Mass: 242.93535
- Molecular Formula: C8H6BrNOS
- Molecular Weight: 244.11
- SMILES: C1=C(SC2=CN=CC(=C21)Br)CO
- Topological: 61.4
- Monoisotopic Mass: 242.93535
- Synonyms: (4-bromothieno[2,3-c]pyridin-2-yl)methanol, 870243-94-0, MFCD12923087, SCHEMBL5555026, AKOS030632729, DS-19270, DB-160778, CS-0162269, C76842
Application
(4-Bromothieno[2,3-c]pyridin-2-yl)methanol serves as a versatile intermediate in medicinal chemistry for the synthesis of bioactive molecules targeting kinase inhibition or CNS disorders. Its bromine moiety enables palladium-catalyzed cross-coupling reactions (e.g., Suzuki, Heck) for structural diversification. Researchers also utilize this compound in the development of fluorescent probes and organic electronic materials due to its conjugated thienopyridine scaffold.
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