Description

1-[3-(Trifluoromethyl)phenyl]propan-1-ol (CAS No. 618-97-3) is a high-purity fluorinated aromatic alcohol with the molecular formula C₁₀H₁₁F₃O. This compound features a trifluoromethyl (–CF₃) group at the meta position of the phenyl ring, enhancing its electron-withdrawing properties and making it a valuable intermediate in organic synthesis and pharmaceutical research. Its propanol-1-ol chain provides reactivity for further derivatization, such as esterification or oxidation. Ideal for researchers in medicinal chemistry, material science, and agrochemical development, this product is supplied with rigorous QC validation (≥98% purity by GC/HPLC) to ensure consistency in your experiments. Store in a cool, dry place under inert conditions to maintain stability.

Properties

• CAS Number: 618-97-3
• Complexity: 179
• IUPAC Name: 1-[3-(trifluoromethyl)phenyl]propan-1-ol
• InChI: InChI=1S/C10H11F3O/c1-2-9(14)7-4-3-5-8(6-7)10(11,12)13/h3-6,9,14H,2H2,1H3
• InChI Key: SZSJCUKIEPGUMF-UHFFFAOYSA-N
• Exact Mass: 204.07619946
• Molecular Formula: C10H11F3O
• Molecular Weight: 204.19
• SMILES: CCC(C1=CC(=CC=C1)C(F)(F)F)O
• Topological: 20.2
• Monoisotopic Mass: 204.07619946
• Synonyms: 618-97-3, 1-((3-Trifluoromethyl)phenyl)propanol-1, 1-[(3-Trifluoromethyl)phenyl]propanol-1, 1-[3-(trifluoromethyl)phenyl]propanol-1, 1-(3-(trifluoromethyl)phenyl)propan-1-ol, 1-[3-(trifluoromethyl)phenyl]propan-1-ol, 1-[3-(trifluoromethyl)phenyl]-1-propanol, SCHEMBL4669029, SCHEMBL18242268, DTXSID60977380, SZSJCUKIEPGUMF-UHFFFAOYSA-N, MFCD00046668, SBB093287, AKOS009159145, DB-054016, CS-0326858, N12228, 3-(1-Hydroxyprop-1-yl)benzotrifluoride, alpha-Ethyl-3-(trifluoromethyl)benzyl alcohol

Application

1-[3-(Trifluoromethyl)phenyl]propan-1-ol is widely used as a key building block in the synthesis of pharmaceuticals, particularly for compounds targeting CNS disorders due to its fluorinated aromatic structure. It serves as a precursor for liquid crystals and advanced materials, leveraging the –CF₃ group’s polarity and thermal stability. Researchers also employ it in catalysis studies and as a chiral auxiliary in asymmetric synthesis.

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