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CAS 175276-66-1

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5-Methyl-2-(trifluoromethyl)furan-3-carbonyl chloride

Description:
5-Methyl-2-(trifluoromethyl)furan-3-carbonyl chloride is an organic compound characterized by its furan ring structure, which is a five-membered aromatic ring containing oxygen. The presence of a methyl group and a trifluoromethyl group on the furan ring significantly influences its chemical reactivity and physical properties. The carbonyl chloride functional group (–COCl) indicates that this compound is a type of acyl chloride, which is known for its reactivity, particularly in nucleophilic acyl substitution reactions. This compound is likely to be a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is soluble in organic solvents but may have limited solubility in water due to the hydrophobic nature of the furan ring and the trifluoromethyl group. The trifluoromethyl group imparts unique electronic properties, making the compound potentially useful in various synthetic applications, including pharmaceuticals and agrochemicals. However, due to the presence of the carbonyl chloride moiety, it should be handled with care, as it can be corrosive and reactive with water and amines.
Formula:C7H4ClF3O2
InChI:InChI=1/C7H4ClF3O2/c1-3-2-4(6(8)12)5(13-3)7(9,10)11/h2H,1H3
InChI key:InChIKey=YJUNYUKKNWEHBQ-UHFFFAOYSA-N
SMILES:C(Cl)(=O)C1=C(C(F)(F)F)OC(C)=C1
Synonyms:
  • 3-Furancarbonyl chloride, 5-methyl-2-(trifluoromethyl)-
  • 5-Methyl-2-(trifluoromethyl)furan-3-carbonyl chloride
  • 5-Methyl-2-(trifluoromethyl)-3-furancarbonyl chloride
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