20199-06-8

Basic information

• Product Name: 4-methyl-N-phenylbenzenecarbothioamide
• CAS NO: 20199-06-8
• Molecular Formula: C₁₄H₁₃NS
• Molecular Weight: 227.3247
• Mol File: 20199-06-8.mol
• Article Data: 16

Chemical Properties

• Boiling Point: 343.6°C at 760 mmHg
• Flash Point: 161.6°C
• Density: 1.181g/cm³
• Vapor Pressure: 6.95E-05mmHg at 25°C
• Refractive Index: 1.682
• CAS DataBase Reference: 4-methyl-N-phenylbenzenecarbothioamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methyl-N-phenylbenzenecarbothioamide(20199-06-8)
• EPA Substance Registry System: 4-methyl-N-phenylbenzenecarbothioamide(20199-06-8)

Safety Data

• Hazardous Substances Data: 20199-06-8(Hazardous Substances Data)

Upstream product

• 103-72-0 phenyl isothiocyanate 
• 108-88-3 toluene 
• 2168-80-1 4-methyldithioic acid 
• 62-53-3 aniline 
• 6833-18-7 4-methyl-N-phenylbenzamide 
• 133218-28-7 p-Methyl-N-(3-phenylpropionyl)thiobenzanilide 
• 60410-77-7 bis(4-methylbenzenethiocarbonyl) sulphide 
• 64586-19-2 Acetic 4-methylthiobenzoic thioanhydride 
• 97270-52-5 4-(methyl)thiobenzoyl diphenylthiophosphinoyl sulfide 
• 97270-58-1 4-(methyl)thiobenzoyl diphenylselenophosphinoyl sulfide 
• 120449-42-5 Se-phenyl 4-methylbenzenecarboselenothioate 
• 42967-76-0 piperidinium 4-methylbenzenecarbodithiolate 
• 53724-36-0 sodium 4-(methyl)dithiobenzoate 
• 74670-57-8 cesium 4-methylbenzenecarbodithioate 

Downstream Products

• 16112-21-3 2-(4-methylphenyl)-1,3-benzothiazole 
• 20199-07-9 Thio-p-toluylanilin-S-oxyd; N-(4-Methyl-thiobenzoyl)-anilin-S-oxyd 
• 133218-28-7 p-Methyl-N-(3-phenylpropionyl)thiobenzanilide 
• 6833-18-7 4-methyl-N-phenylbenzamide 
• 136169-27-2 C₁₅H₁₆N₄S 
• 83078-39-1 4-methyl-thiobenzoic acid O-benzyl ester 

Relevant articles and documents

Visible-Light Carbon Nitride-Catalyzed Aerobic Cyclization of Thiobenzanilides under Ambient Air Conditions

A metal-free heterogeneous photocatalysis has been developed for the synthesis of benzothiazoles via intramolecular C-H functionalization/C-S bond formation of thiobenzanilides by inexpensive graphitic carbon nitride (g-C3N4) under visible-light irradiation. This reaction provides access to a broad range of 2-substituted benzothiazoles in high yields under an air atmosphere at room temperature without addition of a strong base or organic oxidizing reagents. In addition, the catalyst was found to be stable and reusable after five reaction cycles.

Method for promoting elemental sulfur to synthesize thioamide by mixed alkali in water phase

The invention provides a method for promoting elemental sulfur to synthesize a thioamide compound by a mixed alkali in a water phase, and belongs to the field of organic synthesis. According to the method, an aldehyde compound and an amide compound are us

Functionalization of activated methylene C-H bonds with nitroarenes and sulfur for the synthesis of thioamides

We report a method to obtain arylthioamides by the functionalization of sp3 C-H bonds in phenylacetic acids and benzyl alcohols. Reactions proceeded without the use of any solvents and were compatible with many functionalities and heterocycles. These conditions allow for a rapid synthesis of thioamides from simple, commercial substrates.