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(3-(2-Fluorophenyl)-1,2,4-oxadiazol-5-yl)methanamine

  • CAS No. 919017-55-3

  • Cat. No. CS-0461780
  • Molecule weightNone
  • Purity≥95%
  • MDL No.MFCD08899396

*For research and further manufacturing use only, not for direct human use.

(3-(2-Fluorophenyl)-1,2,4-oxadiazol-5-yl)methanamine|CS-0461780

Structure of 919017-55-3

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General Information

  • CAS No. 919017-55-3
  • Cat. No. CS-0461780
  • Purity ≥95%
  • MDL No. MFCD08899396
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₈FN₃O
  • Molecular Weight None
  • Synonym(s) [3-(2-fluorophenyl)-1,2,4-oxadiazol-5-yl]methanamine
  • SMILES C1=CC=C(C(=C1)C2=NOC(=N2)CN)F

Description

This oxadiazole derivative features a 2-fluorophenyl group conjugated to a methanamine side chain, delivering enhanced electron-withdrawing character and improved solubility. The para-fluoro substitution stabilizes the aromatic system while facilitating downstream functionalization. Ideal for medicinal chemistry applications requiring metabolic stability and targeted binding.

Application

(3-(2-Fluorophenyl)-1,2,4-oxadiazol-5-yl)methanamine serves as a versatile building block for medicinal chemistry, enabling the construction of bioactive heterocycles through standard coupling reactions. Its oxadiazole core offers enhanced metabolic stability and favorable polarity, while the primary amine facilitates conjugation with carboxylic acids, aldehydes, or isocyanates. Bench-stable and readily purified by chromatography, it functions effectively in parallel synthesis campaigns targeting CNS-directed therapeutics and kinase inhibitors.

Safety Information

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Computational Chemistry Data

  • TPSA   64.94
  • LogP   1.3344
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   2

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