CAS 1030-27-9

3-(4-(dimethylamino)phenyl)-1-phenylprop-2-en-1-one

Description:

3-(4-(Dimethylamino)phenyl)-1-phenylprop-2-en-1-one, commonly referred to as a type of chalcone, is an organic compound characterized by its conjugated double bond system, which contributes to its potential as a chromophore. This compound features a dimethylamino group, which enhances its electron-donating properties, making it more reactive in various chemical reactions. The presence of both phenyl and prop-2-en-1-one moieties suggests that it may exhibit interesting photophysical properties, including fluorescence, and could be utilized in dye applications or as a precursor in organic synthesis. Additionally, chalcones are known for their biological activities, including anti-inflammatory and antimicrobial properties, which may be relevant for pharmaceutical research. The compound's structure allows for various substitution patterns, influencing its solubility and reactivity. Overall, 3-(4-(dimethylamino)phenyl)-1-phenylprop-2-en-1-one is a versatile compound with potential applications in materials science and medicinal chemistry.

Formula: C₁₇H₁₇NO

InChI: InChI=1/C17H17NO/c1-18(2)16-11-8-14(9-12-16)10-13-17(19)15-6-4-3-5-7-15/h3-13H,1-2H3/b13-10+

Synonyms:

• Dimethylaminochalcone
• 4-(Dimethylamino)benzalacetophenone
• 4-Dimethylamino chalcone
• Ai3-22121
• Ccris 2223
• Nsc 229037
• Nsc 360
• Nsc 40308
• p-(Dimethylamino)styryl phenyl ketone
• 2-Propen-1-one, 3-(4-(dimethylamino)phenyl)-1-phenyl- (9CI)
• 4-Dimethylaminochalcone
• Chalcone, 4-(dimethylamino)- (8CI)

4-(Dimethylamino)chalcone

CAS: 1030-27-9

4-(Dimethylamino)chalcone

Formula: C₁₇H₁₇NO

Purity: ≥95%

Color and Shape: orange to dark red crsytalline solid

Molecular weight: 251.32g/mol

Ref: 54-OR27791

4-(Dimethylamino)chalcone

CAS: 1030-27-9

4-(Dimethylamino)chalcone is a fluorescent molecule that has been used as a fluorescence probe to study the structures of fatty acids and other molecules. It is also used to detect neutral pH in biological studies. 4-(Dimethylamino)chalcone reacts with carbonyl groups to form stable complexes, which are useful for structural analysis. The fluorescence intensity is proportional to the concentration of the carbonyl group. This molecule has been shown to be potently active against human serum, which may be due to its ability to bind with protein and form stable complexes.

Formula: C₁₇H₁₇NO

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 251.32 g/mol

Ref: 3D-FD55268

4-(Dimethylamino)chalcone

CAS: 1030-27-9

Formula: C₁₇H₁₇NO

Molecular weight: 251.329

Ref: 10-F494190