Description

2-Propanol, 1-[4-(1-methylpropyl)phenoxy]-3-(2,2,3,3-tetrafluoropropoxy)- (CAS No. 308362-88-1) is a high-purity fluorinated organic compound with the molecular formula C₁₆H₂₂F₄O₃. This specialty chemical is designed for advanced research and industrial applications, offering exceptional stability and reactivity due to its unique tetrafluoropropoxy and phenoxy functional groups. Its IUPAC name is 1-(4-butan-2-ylphenoxy)-3-(2,2,3,3-tetrafluoropropoxy)propan-2-ol. The compound is rigorously tested for quality, ensuring >98% purity by HPLC, and is supplied in sealed, light-resistant containers to maintain integrity. Ideal for synthetic chemistry, material science, and pharmaceutical research, this product is a valuable tool for developing novel fluorinated materials or intermediates.

Properties

• CAS Number: 308362-88-1
• Complexity: 320
• IUPAC Name: 1-(4-sec-butylphenoxy)-3-(2,2,3,3-tetrafluoropropoxy)propan-2-ol
• InChI: InChI=1S/C16H22F4O3/c1-3-11(2)12-4-6-14(7-5-12)23-9-13(21)8-22-10-16(19,20)15(17)18/h4-7,11,13,15,21H,3,8-10H2,1-2H3
• InChI Key: CJBQJVABOFLHNY-UHFFFAOYSA-N
• Exact Mass: 338.15050721
• Molecular Formula: C16H22F4O3
• Molecular Weight: 338.34
• SMILES: CCC(C)C1=CC=C(C=C1)OCC(COCC(C(F)F)(F)F)O
• Topological: 38.7
• Monoisotopic Mass: 338.15050721
• Synonyms: DTXSID70889167, 2-Propanol, 1-(4-(1-methylpropyl)phenoxy)-3-(2,2,3,3-tetrafluoropropoxy)-, 2-Propanol, 1-[4-(1-methylpropyl)phenoxy]-3-(2,2,3,3-tetrafluoropropoxy)-, DTXCID201028435, 308362-88-1, 1-(2,2,3,3-Tetrafluoropropoxy)-3-(4-sec-butylphenoxy)-2-propanol, 1-(4-Sec-Butylphenoxy)-3-(2,2,3,3-Tetrafluoropropoxy)-2-Propanol, SCHEMBL2108251, MFCD09907684, 1-(2,2,3,3-tetrafluoropropoxy)-3-(4-s-butylphenoxy)-2-propanol, 1-(2,2,3,3,-Tetrafluoropropoxy)-3-(4- sec-butylphenoxy)-2-propanol, 1-(2,2,3,3,-Tetrafluoropropoxy)-3-(4-sec-butylphenoxy)-2-propanol, 1-(4-butan-2-ylphenoxy)-3-(2,2,3,3-tetrafluoropropoxy)propan-2-ol

Application

This fluorinated propanol derivative is widely used as an intermediate in the synthesis of specialty polymers and surfactants, leveraging its unique fluorinated side chain for enhanced hydrophobicity and chemical resistance. Researchers employ it in the development of advanced coatings, adhesives, and electronic materials due to its thermal stability and low surface energy. Additionally, it serves as a key building block in pharmaceutical and agrochemical research for introducing fluorinated moieties into bioactive molecules.

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