Atomfair Beflubutamid C18H17F4NO2

Description Beflubutamid (CAS No. 113614-09-8) is a high-purity fluorinated phenoxybutanamide compound with the molecular formula C18H17F4NO2and IUPAC name N-benzyl-2-[4-fluoro-3-(trifluoromethyl)phenoxy]butanamide . This specialized chemical is rigorously synthesized for research applications, featuring a unique trifluoromethyl-phenoxy backbone that enhances its biochemical interactions. Provided as a crystalline solid with ??95% purity (HPLC), it is ideal for structure-activity relationship (SAR) studies, agrochemical development, and metabolic pathway investigations. Each batch undergoes comprehensive QC testing (NMR, LC/MS) to ensure consistency. Store at 2-8??C in amber vials under inert atmosphere to maintain stability.

Description

Description

Beflubutamid (CAS No. 113614-09-8) is a high-purity fluorinated phenoxybutanamide compound with the molecular formula C18H17F4NO2 and IUPAC name N-benzyl-2-[4-fluoro-3-(trifluoromethyl)phenoxy]butanamide. This specialized chemical is rigorously synthesized for research applications, featuring a unique trifluoromethyl-phenoxy backbone that enhances its biochemical interactions. Provided as a crystalline solid with ??95% purity (HPLC), it is ideal for structure-activity relationship (SAR) studies, agrochemical development, and metabolic pathway investigations. Each batch undergoes comprehensive QC testing (NMR, LC/MS) to ensure consistency. Store at 2-8??C in amber vials under inert atmosphere to maintain stability.

  • CAS No: 113614-09-8
  • Molecular Formula: C18H17F4NO2
  • Molecular Weight: 355.3
  • Exact Mass: 355.11954143
  • Monoisotopic Mass: 355.11954143
  • IUPAC Name: N-benzyl-2-[4-fluoro-3-(trifluoromethyl)phenoxy]butanamide
  • SMILES: CCC(C(=O)NCC1=CC=CC=C1)OC2=CC(=C(C=C2)F)C(F)(F)F
  • Synonyms: Beflubutamid, 113614-08-7, Beflubutamid [ISO], YW9853IQ3U, BENFLUAMID

Application

Beflubutamid is primarily investigated as a protoporphyrinogen oxidase (PPO) inhibitor for herbicide development targeting broadleaf weeds. Researchers utilize it to study fluorinated phenoxy compounds’ mode of action in plant metabolic disruption. Its trifluoromethyl group makes it valuable for probing xenobiotic metabolism in agricultural toxicology studies.

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