5706-83-2

Basic information

• Product Name: 3-[3-(benzyloxy)phenyl]-1-(3,4,5-trimethoxyphenyl)prop-2-en-1-one
• CAS NO: 5706-83-2
• Molecular Formula: C₉H₁₁N₃S
• Molecular Weight: 404.4551
• Mol File: 5706-83-2.mol
• Article Data: 44

Chemical Properties

• Boiling Point: 586°C at 760 mmHg
• Flash Point: 253.4°C
• Density: 1.167g/cm³
• Vapor Pressure: 1.03E-13mmHg at 25°C
• Refractive Index: 1.598
• CAS DataBase Reference: 3-[3-(benzyloxy)phenyl]-1-(3,4,5-trimethoxyphenyl)prop-2-en-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-[3-(benzyloxy)phenyl]-1-(3,4,5-trimethoxyphenyl)prop-2-en-1-one(5706-83-2)
• EPA Substance Registry System: 3-[3-(benzyloxy)phenyl]-1-(3,4,5-trimethoxyphenyl)prop-2-en-1-one(5706-83-2)

Safety Data

• Hazardous Substances Data: 5706-83-2(Hazardous Substances Data)

Upstream product

• 104-87-0 4-methyl-benzaldehyde 
• 79-19-6 thiosemicarbazide 
• 83639-13-8 2,4-bis(4-methylphenyl)-3-azabicyclo[3.3.1]nonan-9-one 
• 4346-94-5 thiosemicarbazide hydrochloride 
• 45708-98-3 p-Toluylaldehyd-imin 

Downstream Products

• 26907-54-0 2-amino-5-(4-methylphenyl)-1,3,4-thiadiazole 
• 104-87-0 4-methyl-benzaldehyde 
• 171628-39-0 2-(2-(4-methylbenzylidene)hydrazinyl)-4-phenylthiazole 
• 935853-30-8 C₁₈H₁₄N₄SO 
• 87220-07-3 5-Phenyl-3-p-tolyl-thiazolo[2,3-c][1,2,4]triazole 
• 87245-81-6 5-p-Chlorophenyl-3-p-tolylthiazolo<2.3-c>-s-triazole 
• 40288-18-4 2-chloro-5-(p-tolyl)-1,3,4-thiadiazole 

Relevant articles and documents

Synthesis, antimicrobial and antioxidant evaluation with in silico studies of new thiazole Schiff base derivatives

A series of nineteen thiazole Schiff base derivatives 2a-2s were synthesized (Scheme 1) and elucidated by spectral analyses (IR, 1H NMR and HRMS). The evaluation of their antimicrobial activities against two gram-positive, two gram-negative, an

Assessment of Thiosemicarbazone-Containing Compounds as Potential Antileukemia Agents against P-gp Overexpressing Drug Resistant K562/A02 Cells

P-Glycoprotein (P-gp) overexpression is considered to be the leading cause of multidrug resistance (MDR) and failure of chemotherapy for leukemia. In this study, seventeen thiosemicarbazone-containing compounds were prepared and evaluated as potential ant

Facile synthesis of novel fluorescent thiazole coumarinyl compounds: Electrochemical, time resolve fluorescence, and solvatochromic study

In this study, Benzocoumarin-Thiazoles-Azomethine derivatives with bioactive scaffolds were synthesized and characterized. The present investigation is concerned with the multistep synthesis of thiazole coumarinyl derivatives (5a-k), which were accomplished from naphthaldehyde, ethyl acetoacetate, and thiosemicarbazide. The formation of newly synthesized derivatives was confirmed by 1H NMR and 13C NMR spectroscopic studies. Thiazole coumarinyl derivatives were subjected to UV-Visible studies in different solvents such as ethanol, ethyl acetate, and DMF for solvatochromic studies. The synthesized coumarinyl thiazole compounds showed absorption in the range of 332-390 nm. Electrochemical studies were performed in DMSO and redox behavior was offered by thiazoles. Fluorescence of coumarinyl thiazole compounds were examined in ethanol, ethyl acetate, and DMF to visualize the solvent effect on the emitting ability of compounds. Fluorescence spectra of coumarinyl thiazoles expressed a sharp emission in the range 436-550 nm.