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Atomfair 7-Fluoro-3-isopropyl-1H-indazole C10H11FN2

Description 7-Fluoro-3-isopropyl-1H-indazole (CAS No. 1415739-80-8) is a high-purity fluorinated indazole derivative with the molecular formula C10H11FN2. This compound is a valuable heterocyclic building block for pharmaceutical and agrochemical research, featuring a reactive indazole core functionalized with a fluoro group at the 7-position and an isopropyl moiety at the 3-position. Its IUPAC name, 7-fluoro-3-propan-2-yl-2H-indazole , reflects its precise structural configuration. Available in >95% purity (HPLC), this reagent is ideal for medicinal chemistry applications, including kinase inhibitor development and PET tracer synthesis. Supplied in amber vials under inert atmosphere to ensure stability.

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Description

Description

7-Fluoro-3-isopropyl-1H-indazole (CAS No. 1415739-80-8) is a high-purity fluorinated indazole derivative with the molecular formula C10H11FN2. This compound is a valuable heterocyclic building block for pharmaceutical and agrochemical research, featuring a reactive indazole core functionalized with a fluoro group at the 7-position and an isopropyl moiety at the 3-position. Its IUPAC name, 7-fluoro-3-propan-2-yl-2H-indazole, reflects its precise structural configuration. Available in >95% purity (HPLC), this reagent is ideal for medicinal chemistry applications, including kinase inhibitor development and PET tracer synthesis. Supplied in amber vials under inert atmosphere to ensure stability.

  • CAS No: 1415739-80-8
  • Molecular Formula: C10H11FN2
  • Molecular Weight: 178.21
  • Exact Mass: 178.09062652
  • Monoisotopic Mass: 178.09062652
  • IUPAC Name: 7-fluoro-3-propan-2-yl-2H-indazole
  • SMILES: CC(C)C1=C2C=CC=C(C2=NN1)F
  • Synonyms: 7-Fluoro-3-isopropyl-1H-indazole, 1415739-80-8, SCHEMBL14158327, GFKJGIZXOHDIEA-UHFFFAOYSA-N

Application

7-Fluoro-3-isopropyl-1H-indazole serves as a key intermediate in the synthesis of bioactive molecules targeting neurological disorders and oncology pathways. Its fluorinated indazole scaffold demonstrates improved metabolic stability in drug candidates. Researchers utilize this compound in Suzuki-Miyaura cross-coupling reactions to create diversified compound libraries. The isopropyl substitution enhances lipophilicity for blood-brain barrier penetration studies.

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