3-Acetylphenyl isothiocyanate is an organic compound characterized by the presence of both an isothiocyanate functional group and an acetyl group attached to a phenyl ring. Its molecular structure features a phenyl ring substituted at the 3-position with an acetyl group and an isothiocyanate group, which is known for its reactivity and ability to form thiourea derivatives. This compound typically appears as a yellow to brown liquid and has a distinctive pungent odor, characteristic of isothiocyanates. It is soluble in organic solvents but has limited solubility in water. 3-Acetylphenyl isothiocyanate is of interest in various fields, including medicinal chemistry and agricultural science, due to its potential biological activities, including antimicrobial and anticancer properties. As with many isothiocyanates, it may exhibit toxicity, necessitating careful handling and appropriate safety measures during use. Its reactivity allows it to participate in various chemical reactions, making it a valuable intermediate in organic synthesis.

3-Acetylphenyl isothiocyanate

3125-71-1: 3-Isothiocyanatoacetophenone, 1-(3-Isothiocyanatophenyl)Ethanone

3-ACETYLPHENYL ISOTHIOCYANATE

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3-Acetylphenyl isothiocyanate, 97%

1-(3-Isothiocyanatophenyl)ethanone is a synthetic, reagent chemical that belongs to the group of alkenes. It has the chemical groups of an alkene and a nitro group. 1-(3-Isothiocyanatophenyl)ethanone is also a biomolecular with embodied chemistry, which can be mediated by thioformamide as a template. The electrophilicity of 1-(3-isothiocyanatophenyl)ethanone makes it suitable for reactions with azide and nitro groups, which are involved in the synthesis of stereochemically pure compounds.

CAS 3125-71-1: 3-Acetylphenyl isothiocyanate

3-Acetylphenyl isothiocyanate

Ref: 10-F018153

3-ACETYLPHENYL ISOTHIOCYANATE

Ref: IN-DA003ITH

3-Acetylphenyl isothiocyanate, 97%

Ref: 02-L10134

1-(3-Isothiocyanatophenyl)ethanone

Ref: 3D-FI114633