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Atomfair 2-Bromo-3,3,3-trifluoropropan-1-ol C3H4BrF3O

Description 2-Bromo-3,3,3-trifluoropropan-1-ol (CAS No. 311-86-4) is a high-purity fluorinated organic compound with the molecular formula C3H4BrF3O . This specialized chemical is designed for advanced research and industrial applications, offering exceptional reactivity due to its bromo- and trifluoromethyl functional groups. Our product is rigorously tested to meet the highest standards of quality, ensuring consistency in synthetic and medicinal chemistry workflows. Ideal for nucleophilic substitution reactions, cross-coupling, and fluorination studies, this compound is supplied in sealed containers under inert conditions to guarantee stability and longevity. Researchers can rely on its precise composition for developing pharmaceuticals, agrochemicals, and specialty materials.

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Description

Description

2-Bromo-3,3,3-trifluoropropan-1-ol (CAS No. 311-86-4) is a high-purity fluorinated organic compound with the molecular formula C3H4BrF3O. This specialized chemical is designed for advanced research and industrial applications, offering exceptional reactivity due to its bromo- and trifluoromethyl functional groups. Our product is rigorously tested to meet the highest standards of quality, ensuring consistency in synthetic and medicinal chemistry workflows. Ideal for nucleophilic substitution reactions, cross-coupling, and fluorination studies, this compound is supplied in sealed containers under inert conditions to guarantee stability and longevity. Researchers can rely on its precise composition for developing pharmaceuticals, agrochemicals, and specialty materials.

  • CAS No: 311-86-4
  • Molecular Formula: C3H4BrF3O
  • Molecular Weight: 192.96
  • Exact Mass: 191.93976
  • Monoisotopic Mass: 191.93976
  • IUPAC Name: 2-bromo-3,3,3-trifluoropropan-1-ol
  • SMILES: C(C(C(F)(F)F)Br)O
  • Synonyms: 2-bromo-3,3,3-trifluoropropan-1-ol, 311-86-4, DTXSID30336480, DTXCID30287569, 688-372-6

Application

2-Bromo-3,3,3-trifluoropropan-1-ol serves as a versatile building block in organic synthesis, particularly in the preparation of fluorinated analogs for drug discovery. Its reactive bromine and hydroxyl groups enable facile derivatization, making it valuable for constructing complex molecules in medicinal chemistry. The trifluoromethyl moiety enhances lipophilicity and metabolic stability, critical for optimizing bioactive compounds. This compound is also employed in materials science for synthesizing fluorinated polymers and liquid crystals.

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