15563-47-0

Basic information

• Product Name: Benzenecarbothioamide, N,N,4-trimethyl-
• CAS NO: 15563-47-0
• Molecular Formula: C10H13NS
• Molecular Weight: 179.286
• Mol File: 15563-47-0.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: Benzenecarbothioamide, N,N,4-trimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenecarbothioamide, N,N,4-trimethyl-(15563-47-0)
• EPA Substance Registry System: Benzenecarbothioamide, N,N,4-trimethyl-(15563-47-0)

Safety Data

• Hazardous Substances Data: 15563-47-0(Hazardous Substances Data)

Upstream product

• 7559-36-6 4-methyl-β-nitrostyrene 
• 68-12-2 N,N-dimethyl-formamide 
• 589-18-4 4-Methylbenzyl alcohol 
• 127-19-5 N,N-dimethyl acetamide 
• 123-11-5 4-methoxy-benzaldehyde 
• 622-97-9 1-ethenyl-4-methylbenzene 
• 124-40-3 dimethyl amine 
• 104-87-0 4-methyl-benzaldehyde 
• 3287-02-3 4-(phenylethynyl)toluene 
• 2789-88-0 1,2-bis(4-methylphenyl)acetylene 
• 766-97-2 4-n-methylphenylacetylene 
• 2947-61-7 (4-methylphenyl)acetonitrile 
• 99-94-5 p-Toluic acid 
• 108-88-3 toluene 

Relevant articles and documents

Metal-free three-component synthesis of thioamides from β-nitrostyrenes, amines and elemental sulfur

A metal-free C[dbnd]C bond cleavage reaction of β-nitrostyrenes in the presence of elemental sulfur and secondary amines/amides is described. Elemental sulfur serves as both a raw material and an oxidant for C[dbnd]C bond cleavage, and secondary amines or amides are both feasible nitrogen sources. Besides mild reaction condition and simple work-up procedure, the method provided thioamides with good to excellent yields.

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

Transition-Metal-Free Cleavage of C-C Triple Bonds in Aromatic Alkynes with S8 and Amides Leading to Aryl Thioamides

A novel transition-metal-free cleavage reaction of C-C triple bonds in aromatic alkynes with S8 and amides furnishes aryl thioamides in moderate to excellent yields. The remarkable features of this thioamidation include the metal-free cleavage of C-C triple bond, mild reaction conditions, as well as wide substrate scope that is particularly compatible with some internal aromatic alkynes and acetamides.