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CS-W001157 4
Total: USD 88.00

6-Chloro-2-(trifluoromethyl)nicotinic acid

  • CAS No. 261635-83-0

  • Cat. No. CS-W000652
  • Molecule weightNone
  • Purity≥98%
  • MDL No.MFCD11840271

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

6-Chloro-2-(trifluoromethyl)nicotinic acid|CS-W000652

Structure of 261635-83-0

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General Information

  • CAS No. 261635-83-0
  • Cat. No. CS-W000652
  • Purity ≥98%
  • MDL No. MFCD11840271
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₃ClF₃NO₂
  • Molecular Weight None
  • Synonym(s) 6-chloro-2-(trifluoromethyl)pyridine-3-carboxylic acid
  • SMILES ClC1=NC(C(F)(F)F)=C(C(O)=O)C=C1

Description

6-Chloro-2-(trifluoromethyl)nicotinic acid features a trifluoromethyl group at the 2-position and a chlorine substituent at the 6-position of the nicotinic acid scaffold. This electron-deficient heterocycle serves as a key building block in medicinal chemistry, particularly for developing kinase inhibitors and bioactive compounds requiring enhanced metabolic stability and lipophilic character.

Application

6-Chloro-2-(trifluoromethyl)nicotinic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of biologically active heterocycles and pharmaceutical intermediates. Its electron-deficient pyridine core facilitates nucleophilic aromatic substitution and palladium-catalyzed coupling reactions. The trifluoromethyl group enhances metabolic stability and membrane permeability, while the chloro substituent provides a reliable handle for further functionalization. This compound exhibits excellent bench stability and compatibility with standard purification methods, making it ideal for scalable synthesis workflows.

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Computational Chemistry Data

  • TPSA   50.19
  • LogP   2.452
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   1

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