76579-52-7

Basic information

• Product Name: Benzeneethanethioamide, 4-methoxy-N,N-dimethyl-
• Synonyms: Benzeneethanethioamide, 4-methoxy-N,N-dimethyl-
• CAS NO: 76579-52-7
• Molecular Formula: C₁₁H₁₅NOS
• Molecular Weight: 209.3079
• Mol File: 76579-52-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 307.4°Cat760mmHg
• Flash Point: 139.7°C
• Appearance: /
• Density: 1.092g/cm³
• Vapor Pressure: 0.000727mmHg at 25°C
• Refractive Index: 1.569
• CAS DataBase Reference: Benzeneethanethioamide, 4-methoxy-N,N-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneethanethioamide, 4-methoxy-N,N-dimethyl-(76579-52-7)
• EPA Substance Registry System: Benzeneethanethioamide, 4-methoxy-N,N-dimethyl-(76579-52-7)

Safety Data

• Hazardous Substances Data: 76579-52-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H15NOS/c1-12(2)11(14)8-9-4-6-10(13-3)7-5-9/h4-7H,8H2,1-3H3

Upstream product

• 124-40-3 dimethyl amine 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 4137-10-4 DIMCARB 
• 830-09-1 3-(4'-methoxyphenyl)propenoic acid 
• 68-12-2 N,N-dimethyl-formamide 
• 104-47-2 p-methoxybenzylnitrile 
• 35453-06-6 4-methoxy-β-methylsulfinyl-β-methylthiostyrene 

Downstream Products

• 775-33-7 4-methoxyphenethyl-dimethylamine 
• 104-01-8 4-Methoxyphenylacetic acid 
• 124-40-3 dimethyl amine 
• 131801-70-2 N,N-dimethyl-α-(1-hydroxycyclohexyl)-p-methoxyphenylthioacetamide 
• 539-15-1 N,N-dimethyltyramine 

Relevant articles and documents

Sulfur promoted decarboxylative thioamidation of carboxylic acids using formamides as amine proxy

An efficient decarboxylative thioamidation of arylacetic and cinnamic acids has been developed employing formamides as amine surrogate and sulfur as promoter. Thioamides with variant structural features are obtained under mild reaction conditions without the use of transition metal catalysts and oxidants.

Dimethylammonium Dimethylcarbamate - A Useful Reagent for the Willgerodt-Kindler Reaction

Dimethylammonium dimethylcarbamate (dimcarb), easily accessible from dimethylamine and carbon dioxide, is a useful reagent for the Willgerodt-Kindler synthesis of N,N-dimethylthiocarboxamides.Moreover, dimcarb displays some unusual properties, and generally behaves as a preparatively useful dimethylamine source.