1-(3,4-Diaminophenyl)ethanone, also known as 3,4-diaminoacetophenone, is an organic compound characterized by the presence of an acetophenone structure with two amino groups located at the 3 and 4 positions of the phenyl ring. This compound typically appears as a solid and is soluble in polar solvents due to the presence of amino groups, which can engage in hydrogen bonding. It has applications in organic synthesis, particularly in the production of dyes and pharmaceuticals, owing to its ability to undergo various chemical reactions, such as acylation and diazotization. The amino groups contribute to its reactivity, making it a versatile intermediate in the synthesis of more complex molecules. Additionally, the compound may exhibit biological activity, which can be explored for potential therapeutic uses. Safety data should be consulted, as compounds with amino groups can sometimes pose health risks, including potential toxicity or allergenic properties. Proper handling and storage conditions are essential to ensure safety during use.

1-(3,4-Diaminophenyl)ethanone

21304-39-2: 1-(3,4-Diaminophenyl)ethan-1-one, 1-(3,4-Diaminophenyl)ethanone, 3',4'-Diaminoacetophenone, 3′,4′-Diaminoacetophenone, 4-Acetyl-1,2-phenylenediamine, Acetophenone, 3',4'-diamino- (8CI), Acetophenone, 3,4-diamino-, Acetophenone,3,4-diamino- (4CI), p-Acetyl-o-phenylenediamine, Ethanone, 1-(3,4-diaminophenyl)-

1-(3,4-Diamino-phenyl)ethanone

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CAS 21304-39-2: 1-(3,4-Diaminophenyl)ethanone

1-(3,4-Diamino-phenyl)ethanone

Ref: 54-OR97656

3',4'-Diaminoacetophenone

Ref: 3D-FD106489

1-(3,4-Diaminophenyl)ethanone

Ref: 10-F336632