114569-19-6

Basic information

• Product Name: 1-{4-[(4-hydroxybenzylidene)amino]phenyl}ethanone
• Synonyms: 1-{4-[(4-hydroxybenzylidene)amino]phenyl}ethanone
• CAS NO: 114569-19-6
• Molecular Formula: C₁₅H₁₃NO₂
• Molecular Weight: 239.26922
• Mol File: 114569-19-6.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-{4-[(4-hydroxybenzylidene)amino]phenyl}ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-{4-[(4-hydroxybenzylidene)amino]phenyl}ethanone(114569-19-6)
• EPA Substance Registry System: 1-{4-[(4-hydroxybenzylidene)amino]phenyl}ethanone(114569-19-6)

Safety Data

• Hazardous Substances Data: 114569-19-6(Hazardous Substances Data)

Upstream product

• 123-08-0 4-hydroxy-benzaldehyde 
• 99-92-3 p-aminobenzophenone 
• 64-17-5 ethanol 

Downstream Products

• 131888-14-7 (E)-1-(4′-aminophenyl)-3-(4-methoxyphenyl)prop-2-en-1-one 
• 126443-09-2 1-(4-aminophenyl)-3-<4-(dimethylamino)phenyl>prop-2-en-1-one 
• 25870-76-2 1-(4-aminophenyl)-3-(4-cyanophenyl)prop-2-en-1-one 
• 2403-30-7 (E)-1-(4-aminophenyl)-3-phenylprop-2-en-1-one 
• 569646-59-9 (2E)-1-(4′-aminophenyl)-3-(4-chlorophenyl)prop-2-en-1-one 
• 569646-61-3 (E)-1-(4′-aminophenyl)-3-(4-methylphenyl)prop-2-en-1-one 
• 876048-06-5 (E)-1-(4'-aminophenyl)-3-(3-bromophenyl)-2-propen-1-one 
• 1370225-46-9 C₂₄H₁₉ClN₄O 
• 3785-90-8 2-(4-hydroxyphenylmethylene)malononitrile 
• 51947-45-6 dimethyl (4-hydroxyphenyl)methylenemalonate 
• 115848-64-1 3-(4-acetophenyl)-2-(p-hydroxyphenyl)thiazolidin-4-one 

Relevant articles and documents

Design, synthesis and in vitro antimalarial evaluation of new quinolinylhydrazone derivatives

A series of novel quinolinylhydrazones (5a-f) was synthesized by the condensation reaction of 2,6-diaryl-substituted piperidin-4-ones (4a-f) with 7-chloro-4-hydrazinoquinoline (2). Novel quinolinylhydrazones containing Shiff bases 8a-f and 11a-f were obta

Highly efficient synthesis and characterization of the GPR30-selective agonist G-1 and related tetrahydroquinoline analogs

The GPR30 agonist probe G-1 and structural analogs were efficiently synthesized using multicomponent or stepwise Sc(iii)-catalyzed aza-Diels-Alder cyclization. Optimization of solvent and reaction temperature provided enhanced endo-diastereoselectivity.

Solid phase synthesis of aminochalcones

A microwave-assisted solid phase synthesis of aminochalcones via the Claisen-Schmidt condensation reaction between resin-bound p-aminoacetophenone and aromatic aldehydes was described.

Synthesis of Some New &β-Lactams, 4-Thiazolidinones and Pyrazolines

N-Arylidene-p-aminoacetophenone (I) and N-arylidene-4'-aminochalcones (V) have been converted into a series of substituted β-lactams (III) and 4-thiazolidinones (IV), and pyrazolines (VI, VII) respectively. p-Chloroacetamidoacetophenone (II) has also been converted into series of substituted 4'-piperidino/morpholinoacetoamidochalcones (X) which undergo cyclization on treatment with hydrazine, phenylhydrazine or thiourea to pyrazolines (XI, XII) and pyrimidine-2-thiones (XIII) respectively.The antibacterial and antifungal activities of the compounds have been determined.