6335-93-9

Basic information

• Product Name: 1-(2-NAPHTHYL)-3-PHENYL-2-THIOUREA
• Synonyms: 1-(2-NAPHTHYL)-3-PHENYL-2-THIOUREA
• CAS NO: 6335-93-9
• Molecular Formula: C₁₇H₁₄N₂S
• Molecular Weight: 278.37146
• Mol File: 6335-93-9.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 442°Cat760mmHg
• Flash Point: 221.1°C
• Appearance: /
• Density: 1.314g/cm³
• Vapor Pressure: 5.21E-08mmHg at 25°C
• Refractive Index: 1.795
• CAS DataBase Reference: 1-(2-NAPHTHYL)-3-PHENYL-2-THIOUREA(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-NAPHTHYL)-3-PHENYL-2-THIOUREA(6335-93-9)
• EPA Substance Registry System: 1-(2-NAPHTHYL)-3-PHENYL-2-THIOUREA(6335-93-9)

Safety Data

• Hazardous Substances Data: 6335-93-9(Hazardous Substances Data)

Usage

Chemical structure

Thiourea derivative with a naphthyl and a phenyl group attached to the nitrogen and sulfur atoms, respectively.

Potential applications

Medicinal chemistry
Agriculture
Materials science

Biological activity

Antifungal properties
Antibacterial properties

Pharmaceutical development

Potential candidate for the development of new pharmaceuticals due to its antifungal and antibacterial properties.

Agrochemical development

Potential candidate for the development of new agrochemicals due to its antifungal and antibacterial properties.

Material synthesis

Unique structural features make it a promising candidate for the synthesis of novel materials with specific properties.

Further research

More research is needed to explore its full potential and possible applications in different industries.

InChI:InChI=1/C17H14N2S/c20-17(18-15-8-2-1-3-9-15)19-16-11-10-13-6-4-5-7-14(13)12-16/h1-12H,(H2,18,19,20)

Upstream product

• 103-72-0 phenyl isothiocyanate 
• 91-59-8 naphthalen-2-ylamine 
• 67-66-3 chloroform 
• 62-53-3 aniline 
• 1166-32-1 N,N'-di(2-naphthyl)thiourea 
• 1636-33-5 2-naphthyl isothiocyanate 

Downstream Products

• 7669-45-6 (3-naphthalen-2-yl-4-oxo-2-phenylimino-thiazolidin-5-yl)-acetic acid 
• 1636-33-5 2-naphthyl isothiocyanate 
• 103-72-0 phenyl isothiocyanate 
• 3394-04-5 naphthalen-2-yl-thiourea 
• 1056051-20-7 [4-(3,4-dimethoxyphenyl)-thiazol-2-yl]-naphthalen-2-yl-amine 
• 111091-98-6 N-methyl-N-phenylnaphtho[2,1-d]thiazol-2-amine 
• 114854-04-5 1,3-dihydro-5-1-(4',6'-dimethoxypyrimidin-2'-yl)-p-sulphamylbenzeneazo>-1-(2'-naphthyl)-3-phenyl-2-thioxo-2H,5H-pyrimidine-4,6-dione 
• 114900-53-7 1,3-dihydro-5-1-(1'-phenylpyrazol-5'-yl)-p-sulphamylbenzeneazo>-1-(2'-naphthyl)-3-phenyl-2-thioxo-2H,5H-pyrimidine-4,6-dione 
• 114871-64-6 1,3-dihydro-5-1-(5'-methyl-1',3',4'-thiadiazol-2'-yl)-p-sulphamylbenzeneazo>-1-(2'-naphthyl)-3-phenyl-2-thioxo-2H,5H-pyrimidine-4,6-dione 
• 114854-02-3 1,3-dihydro-5-1-(2',6'-dimethylpyrimidin-4'-yl)-p-sulphamylbenzeneazo>-1-(2'-naphthyl)-3-phenyl-2-thioxo-2H,5H-pyrimidine-4,6-dione 
• 114854-03-4 1,3-dihydro-5-1-(4',6'-dimethylpyrimidin-2'-yl)-p-sulphamylbenzeneazo>-1-(2'-naphthyl)-3-phenyl-2-thioxo-2H,5H-pyrimidine-4,6-dione 
• 114854-01-2 1,3-dihydro-5-1-(4'-methylpyrimidin-2'-yl)-p-sulphamylbenzeneazo>-1-(2'-naphthyl)-3-phenyl-2-thioxo-2H,5H-pyrimidine-4,6-dione 
• 114854-00-1 1,3-dihydro-5-1-(m-methoxyphenyl)-p-sulphamylbenzeneazo>-1-(2'-naphthyl)-3-phenyl-2-thioxo-2H,5H-pyrimidine-4,6-dione 
• 114853-97-3 1,3-dihydro-5-1-(o-chlorophenyl)-p-sulphamylbenzeneazo>-1-(2'-naphthyl)-3-phenyl-2-thioxo-2H,5H-pyrimidine-4,6-dione 

Relevant articles and documents

Thiocarbonyl Surrogate via Combination of Sulfur and Chloroform for Thiocarbamide and Oxazolidinethione Construction

An efficient and practical thiocarbonyl surrogate via combination of sulfur and chloroform has been developed. A variety of thiocarbamides and oxazolidinethiones have been established, including chiral thiourea catalysts and chiral oxazolidinethione auxiliaries with high selectivity. Meanwhile, pesticides Diafenthiuron (an acaricide), ANTU (a rodenticide), and Chloromethiuron (an insecticide) were practically synthesized through this method in gram scale. Dicholorocarbene, as the key intermediate, was further confirmed via a carbene-trapping control experiment.