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Atomfair (2,3,5,6-Tetrafluoro-4-methylphenyl)methanol C8H6F4O CAS 79538-03-7
(2,3,5,6-Tetrafluoro-4-methylphenyl)methanol (CAS No. 79538-03-7) is a fluorinated aromatic alcohol with the molecular formula C8H6F4O . This high-purity compound is characterized by its tetrafluoro-substituted phenyl ring and a hydroxymethyl functional group, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its unique structural properties enhance reactivity and stability, ideal for applications in advanced chemical transformations. Available in various quantities, this product is rigorously tested for quality, ensuring consistency for laboratory and industrial use. Store in a cool, dry place under inert conditions to maintain integrity.
Description
(2,3,5,6-Tetrafluoro-4-methylphenyl)methanol (CAS No. 79538-03-7) is a fluorinated aromatic alcohol with the molecular formula C8H6F4O. This high-purity compound is characterized by its tetrafluoro-substituted phenyl ring and a hydroxymethyl functional group, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its unique structural properties enhance reactivity and stability, ideal for applications in advanced chemical transformations. Available in various quantities, this product is rigorously tested for quality, ensuring consistency for laboratory and industrial use. Store in a cool, dry place under inert conditions to maintain integrity.
Properties
- CAS Number: 79538-03-7
- Complexity: 162
- IUPAC Name: (2,3,5,6-tetrafluoro-4-methyl-phenyl)methanol
- InChI: InChI=1S/C8H6F4O/c1-3-5(9)7(11)4(2-13)8(12)6(3)10/h13H,2H2,1H3
- InChI Key: PJCSTULKVNHEGW-UHFFFAOYSA-N
- Exact Mass: 194.03547746
- Molecular Formula: C8H6F4O
- Molecular Weight: 194.13
- SMILES: CC1=C(C(=C(C(=C1F)F)CO)F)F
- Topological: 20.2
- Monoisotopic Mass: 194.03547746
- Synonyms: 79538-03-7, 2,3,5,6-Tetrafluoro-4-methylbenzyl alcohol, (2,3,5,6-tetrafluoro-4-methylphenyl)methanol, 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol, 2,3,5,6-Tetrafluoro-4-methylbenzylalcohol, MFCD03093260, 2,3,5,6-(Tetrafluoro-4-methylphenyl)methanol;(2,3,5,6-Tetrafluoro-4-methylphenyl)methanol, Benzenemethanol, 2,3,5,6-tetrafluoro-4-methyl-, Tefluthrin metabolite II, 4-methyl-2,3,5,6-tetrafluoro lbenzyl alcohol, (2,3,5,6-tetrafluoro-4-methylphenyl)methan-1-ol, SCHEMBL359368, SCHEMBL1073230, SCHEMBL9311187, tetrafluoro-4-methylbenzylalcohol, DTXSID50370164, PAA00203, SBB063324, AKOS005258017, AC-8277, AS-15858, SY018258, DB-003224, NS00067765, 2,3,5,6-Tetrafluoro-4-methylbenzenemethanol, EN300-7365703, 2,3,5,6-Tetrafluoro-4-methylbenzyl Alcohol; Benzenemethanol, 2,3,5,6-tetrafluoro-4-methyl-; 2,3,5,6-Tetrafluoro-4-methylbenzenemethanol; 2,3,5,6-Tetrafluoro-4-methylbenzyl alcohol; 4-Methyl-2,3,5,6-tetrafluorobenzyl alcohol
Application
(2,3,5,6-Tetrafluoro-4-methylphenyl)methanol is widely used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its electron-withdrawing fluorine atoms enhance the reactivity of the benzyl alcohol group, making it suitable for nucleophilic substitution reactions. Researchers also employ this compound in the development of liquid crystals and specialty polymers due to its thermal and chemical stability. Additionally, it serves as a precursor for advanced materials in electronic and optoelectronic applications.
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