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3-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridine(CAS#956010-87-0)

Chemical Property:

Molecular Formula C7H4F3N3
Molar Mass 187.12
Storage Condition 2-8°C

Product Detail

Product Tags

 3-(trifluoromethyl)-1H-pyrazolo[3,4-b]pyridine(CAS#956010-87-0)

Uses: It is an important intermediate in organic synthesis. In the field of medicinal chemistry, it can be used to synthesize compounds with potential biological activity, and trifluoromethyl and pyrazolopyridine rings in their structures can be modified by various chemical reactions, so as to introduce different pharmacophores to obtain drug molecules with specific pharmacological effects, which may have antibacterial, antiviral, antitumor and other activities. In materials science, it is also possible to prepare organic materials with special properties, such as optoelectronic materials, through further derivatization reactions.
Synthesis method: It has been reported in the literature that 2-fluoropyridine was used as the starting material for the synthesis of multiple grams in one pot by directional ortho-metallization (DOM) technology. This method takes advantage of the special structure of 2-fluoropyridine to introduce trifluoromethyl and construct pyrazolopyridine ring through a series of reactions to obtain the target product. However, the specific synthesis route may vary depending on the raw material and reaction conditions.

Application
3-(Trifluoromethyl)-1H-pyrazolo[3,4-b]pyridine (CAS 956010-87-0) is a heterocyclic building block featuring a fused pyrazole-pyridine core with a trifluoromethyl group at the 3-position. The electron-withdrawing CF3 enhances metabolic stability, lipophilicity, and target binding affinity, making it valuable in medicinal chemistry for developing kinase inhibitors (JAK, BTK, CDK, TBK1) targeting cancer, inflammation, and autoimmune diseases. The NH group enables alkylation or arylation, while the pyridine nitrogen can coordinate to metal ions or participate in hydrogen bonding. This scaffold is also used in agrochemical research, material science, and as a precursor for functionalized heterocycles via cross-coupling or nucleophilic substitution. Xinchem offers custom synthesis, custom chemical synthesis, and contract manufacturing of high-purity this compound with flexible scaling from R&D to commercial tons. Contact us today for a competitive quote and reliable global supply.


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