60246-64-2

Basic information

• Product Name: 3-[(2-aminophenyl)sulfanyl]-1,3-diphenylpropan-1-one
• Synonyms: 1-propanone, 3-[(2-aminophenyl)thio]-1,3-diphenyl-; 3-[(2-Aminophenyl)sulfanyl]-1,3-diphenylpropan-1-one; 3-[(2-aminophenyl)thio]-1,3-diphenylpropan-1-one
• CAS NO: 60246-64-2
• Molecular Formula: C₂₁H₁₉NOS
• Molecular Weight: 333.4467
• Mol File: 60246-64-2.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 526.5°C at 760 mmHg
• Flash Point: 272.2°C
• Density: 1.21g/cm³
• Vapor Pressure: 3.55E-11mmHg at 25°C
• Refractive Index: 1.665
• CAS DataBase Reference: 3-[(2-aminophenyl)sulfanyl]-1,3-diphenylpropan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-[(2-aminophenyl)sulfanyl]-1,3-diphenylpropan-1-one(60246-64-2)
• EPA Substance Registry System: 3-[(2-aminophenyl)sulfanyl]-1,3-diphenylpropan-1-one(60246-64-2)

Safety Data

• Hazardous Substances Data: 60246-64-2(Hazardous Substances Data)

Upstream product

• 137-07-5 2-amino-benzenethiol 
• 614-47-1 1,3-diphenyl-propen-3-one 
• 40358-31-4 2,3-dihydro-2,4-diphenyl-1,5-benzothiazepine 
• 94-41-7 benzalacetophenone 

Downstream Products

• 64820-47-9 4-(4-bromophenyl)-2-phenyl-2,3-dihydro-1,5-benzothiazepine 
• 64820-43-5 2,3-dihydro-4-(4-chlorophenyl)-2-phenyl-1,5-benzothiazepine 
• 86602-76-8 2-(4-bromophenyl)-4-phenyl-2,3-dihydro-1,5-benzothiazepine 
• 64820-40-2 2,3-dihydro-4-(4-methoxyphenyl)-2-phenyl-1,5-benzothiazepine 
• 60246-77-7 2-(4-methoxylphenyl)-4-phenyl-2,3-dihydro-1,5-benzothiazepine 
• 60246-82-4 2-(4-chlorophenyl)-4-phenyl-2,3-dihydro-1,5-benzothiazepine 
• 40358-31-4 2,3-dihydro-2,4-diphenyl-1,5-benzothiazepine 
• 137-07-5 2-amino-benzenethiol 
• 985-28-4 1,3-diphenyl-2-propen-1-one 2,4-dinitrophenylhydrazone 

Relevant articles and documents

A practical synthesis of 2,3-dihydro-1,5-benzothiazepines

2,3-Dihydro-1,5-benzothiazepines have been obtained through a domino process involving a Michael addition of 2-aminothiophenols to chalcones, followed by in situ cyclization. Up to 98% chemical yields have been obtained at room temperature under essential

Novel and versatile methodology for synthesis of β-aryl-β- mercapto ketone derivatives as potential urease inhibitors

The objective was to obtain new scaffold of compounds possessing anti-urease activity. For this new and simple method for the synthesis of β-aryl-β-mercapto ketone derivatives based on Michael addition of thiophenol to chalcones in an ionic liquid as a so

Fluoroboric acid adsorbed on silica-gel (HBF4-SiO2) as a new, highly efficient and reusable heterogeneous catalyst for thia-Michael addition to α,β-unsaturated carbonyl compounds

Fluoroboric acid adsorbed on silica-gel (HBF4-SiO2) has been found to be a new and highly efficient heterogeneous catalyst for thia-Michael addition to α,β-unsaturated carbonyl compounds under solvent-free conditions. In the case of