Description
Thieno(3,2-b)pyridin-7-ol (CAS No. 107818-20-2) is a high-purity heterocyclic compound with the molecular formula C7H5NOS. This specialized chemical is widely utilized in pharmaceutical research, organic synthesis, and material science due to its unique thienopyridine scaffold. Our product is rigorously tested for quality, ensuring >94% purity (HPLC) and optimal stability under recommended storage conditions. Ideal for researchers developing novel bioactive molecules, this compound serves as a versatile building block for drug discovery, particularly in kinase inhibitors and CNS-targeting agents. Each batch is supplied with comprehensive analytical data (NMR, MS, HPLC) and handled under strict GMP-compliant protocols to guarantee reproducibility for your critical experiments.
Properties
- CAS Number: 107818-20-2
- Complexity: 190
- IUPAC Name: 4H-thieno[3,2-b]pyridin-7-one
- InChI: InChI=1S/C7H5NOS/c9-6-1-3-8-5-2-4-10-7(5)6/h1-4H,(H,8,9)
- InChI Key: AACVULYSNJAKEQ-UHFFFAOYSA-N
- Exact Mass: 151.00918496
- Molecular Formula: C7H5NOS
- Molecular Weight: 151.19
- SMILES: C1=CNC2=C(C1=O)SC=C2
- Topological: 57.3
- Monoisotopic Mass: 151.00918496
- Synonyms: Thieno[3,2-b]pyridin-7-ol, 107818-20-2, Thieno(3,2-B)pyridin-7-OL, DTXSID20408069, DTXCID90358921, 626-962-7, thieno[3,2-b]pyridin-7(4H)-one, 69627-02-7, 4H-thieno[3,2-b]pyridin-7-one, THIENO(3 2-B)PYRIDIN-7-OL, 7-HYDROXYTHIENO[3,2-B]PYRIDINE, MFCD01863636, thiopheno[3,2-b]pyridin-7-ol, MFCD12964174, BIDD:GT0268, SCHEMBL105581, thieno[3,2,b]pyridin-7-ol, SCHEMBL1497985, SCHEMBL27915712, Thieno-(3,2-B)-pyridin-7-ol, 4H-thieno[3,2-b]pyridine-7-one, BCP27004, CX1280, SBB071463, Thieno[3,2-b]pyridin-7-ol, 94%, AKOS009156544, AKOS015918999, AC-4399, CS-W002859, FS-2637, PB32284, SB10353, ST094914, SY004858, DB-001091, DB-015056, CS-0166785, H1603, EN300-84887, Q27466710, Z1948933786, Thieno[3,2-b]pyridin-7(4H)-one;7-Hydroxythieno[3,2-b]pyridine
Thieno(3,2-b)pyridin-7-ol serves as a key intermediate in the synthesis of pharmacologically active compounds, particularly kinase inhibitors and neuroactive agents. Researchers employ this heterocycle in medicinal chemistry programs targeting protein-protein interactions and allosteric modulation sites. Its fused ring system enables π-stacking interactions in drug design, while the hydroxyl group allows for further functionalization via etherification or cross-coupling reactions. The compound has shown promise in early-stage development of antiviral and anticancer therapeutics.
Safety and Hazards
GHS Hazard Statements
- H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
- H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
- H335 (97.8%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]
Precautionary Statements
- P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501
Hazard Classes and Categories
- Skin Irrit. 2 (100%)
- Eye Irrit. 2 (100%)
- STOT SE 3 (97.8%)
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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.


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