Trifluoroacetone

Trifluoroacetone (1,1,1-trifluoroacetone) is an organofluorine compound with the chemical formula CF3C(O)CH3. ^[1]

7 relations: Acetoacetic acid, Chloroform, Hexafluoroacetone, Journal of Organic Chemistry, Oppenauer oxidation, Organofluorine chemistry, Strecker amino acid synthesis.

Acetoacetic acid

Acetoacetic acid (also diacetic acid) is the organic compound with the formula CH3COCH2COOH.

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Chloroform

Chloroform, or trichloromethane, is an organic compound with formula CHCl3.

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Hexafluoroacetone

Hexafluoroacetone (HFA) is a chemical compound with the formula (CF3)2CO.

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The Journal of Organic Chemistry, colloquially known as JOC or J Org, is a peer-reviewed scientific journal for original contributions of fundamental research in all branches of theory and practice in organic and bioorganic chemistry.

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Oppenauer oxidation

Oppenauer oxidation, named after Rupert Viktor Oppenauer, is a gentle method for selectively oxidizing secondary alcohols to ketones.

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Organofluorine chemistry

Organofluorine chemistry describes the chemistry of the organofluorines, organic compounds that contain the carbon–fluorine bond.

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Strecker amino acid synthesis

The Strecker amino acid synthesis, also known simply as the Strecker synthesis, was discovered by German chemist Adolph Strecker, and is a term used for a series of chemical reactions that synthesize an amino acid from an aldehyde or ketone.

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Redirects here:

1,1,1-trifluoroacetone, 1,1,1-trifluoropropan-2-one, Trifluoracetone.

References

[1] https://en.wikipedia.org/wiki/Trifluoroacetone

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