85660-18-0

Basic information

• Product Name: 4-phenyl-3,4,5,6-tetrahydrobenzo[h]quinazoline-2(1H)-thione
• Synonyms: 4-phenyl-3,4,5,6-tetrahydrobenzo[h]quinazoline-2(1H)-thione;4-phenyl-3,4,5,6-tetrahydrobenzo[h]quinazoline-2-thiol
• CAS NO: 85660-18-0
• Molecular Formula: C₁₈H₁₆N₂S
• Molecular Weight: 292.39804
• Mol File: 85660-18-0.mol
• Article Data: 18

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-phenyl-3,4,5,6-tetrahydrobenzo[h]quinazoline-2(1H)-thione(CAS DataBase Reference)
• NIST Chemistry Reference: 4-phenyl-3,4,5,6-tetrahydrobenzo[h]quinazoline-2(1H)-thione(85660-18-0)
• EPA Substance Registry System: 4-phenyl-3,4,5,6-tetrahydrobenzo[h]quinazoline-2(1H)-thione(85660-18-0)

Safety Data

• Hazardous Substances Data: 85660-18-0(Hazardous Substances Data)

Upstream product

• 100-51-6 benzyl alcohol 
• 6261-32-1 (E)-2-benzylidene-1-tetralone 
• 17356-08-0 thiourea 
• 17216-08-9 2-acetyl-1-tetralone 
• 100-52-7 benzaldehyde 
• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 6261-32-1 2-benzylidene-1-tetralone 

Downstream Products

• 85660-20-4 2-Ethylsulfanyl-4-phenyl-3,4,5,6-tetrahydro-benzo[h]quinazoline; hydrobromide 
• 1141934-87-3 (E)-10-(4-chlorobenzylidene)-7-phenyl-7,10-dihydro-5H-benzo[h]thiazolo[2,3-b]quinazolin-9(6H)-one 
• 1628798-83-3 2-(7-phenyl-6,7-dihydro-5H-benzo[h]thiazolo[2,3-b]-quinazolin-9-yl)-3H-benzo[f]chromen-3-one 
• 1628798-76-4 3-(7-phenyl-6,7-dihydro-5H-benzo[h]thiazolo[2,3-b]-quinazolin-9-yl)-2H-chromen-2-one 
• 1628798-72-0 9-(4-bromophenyl)-7-phenyl-6,7-dihydro-5H-benzo[h]thiazolo-[2,3-b]quinazoline 
• 1628798-67-3 9-(4-chlorophenyl)-7-phenyl-6,7-dihydro-5H-benzo[h]thiazolo-[2,3-b]quinazoline 
• 153258-17-4 5H-5-phenyl-6,7-dihydrothiazolo<2,3-b>benzoquinazolin-3(2H)-one 
• 1440807-79-3 C₂₀H₁₈N₂OS 
• 85660-22-6 2-Ethylsulfanyl-4-phenyl-3,4,5,6-tetrahydro-benzo[h]quinazoline 
• 85660-24-8 2-Ethylsulfanyl-4-phenyl-5,6-dihydro-benzo[h]quinazoline 
• 85660-23-7 2-Methylsulfanyl-4-phenyl-5,6-dihydro-benzo[h]quinazoline 
• 85660-26-0 2-Ethylsulfanyl-4-phenyl-benzo[h]quinazoline 
• 85660-25-9 2-methylmercapto-4-phenylbenzoquinazoline 
• 85660-21-5 2-methylmercapto-4-phenyl-3,4,5,6-tetrahydrobenzoquinazoline 

Relevant articles and documents

Aerobic oxidation of alcohols enabled by nitrogen-doped copper nanoparticle catalysts

Heterogeneous nitrogen-doped carbon-incarcerated copper nanoparticle catalysts have been developed. The catalysts promoted the oxidation of alcohols to the corresponding aldehydes, including aliphatic substrates, in high yield in the presence of an N-oxyl

Base-mediated one-pot synthesis of 3,4,5,6-tetrahydro-4-substituted benzo[h]quinazoline-2(1H)-thione derivatives and evaluation of their antioxidant activity

One-pot three-component Beginelli-like reactions of a ketone 1, an aryl aldehyde 2, and thiourea 3 in the presence of sodium hydroxide are described. In this reaction, 3,4,5,6-tertrahydro-4-substituted quinazoline-2(1H)-thione derivatives 4a–h were obtain

Benzoic acid compound and use thereof

The invention relates to a benzoic acid compound and a use thereof. The benzoic acid compound has a structure shown in the general formula (I) and can be used for treating the hand-foot-mouth disease caused by enterovirus 71 (EV71).