62778-81-8

Basic information

• Product Name: Benzamide, N,N-dimethyl-2-(methylthio)-
• CAS NO: 62778-81-8
• Molecular Formula: C10H13NOS
• Molecular Weight: 195.285
• Mol File: 62778-81-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Benzamide, N,N-dimethyl-2-(methylthio)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N,N-dimethyl-2-(methylthio)-(62778-81-8)
• EPA Substance Registry System: Benzamide, N,N-dimethyl-2-(methylthio)-(62778-81-8)

Safety Data

• Hazardous Substances Data: 62778-81-8(Hazardous Substances Data)

Upstream product

• 65936-04-1 2-Methanesulfinyl-N,N-dimethyl-benzamide 
• 74-88-4 methyl iodide 
• 124-40-3 dimethyl amine 
• 3724-10-5 2-(methylthio)benzoic acid 
• 1442-03-1 2-methylsulfanyl-benzoyl chloride 

Downstream Products

• 73880-49-6 N,N-Dimethyl-<2-(methylthio)benzyl>ammoniumbromid 
• 74484-52-9 dimethyl[(2-methylsulfanyl)benzyl]amine 
• 65936-04-1 2-Methanesulfinyl-N,N-dimethyl-benzamide 
• 73880-58-7 <2-(Dimethylaminomethyl)phenyl>-<(3,3,5,5-tetramethyl-1-trimethylsilyloxycyclohexyl)methyl>-sulfoxid 
• 343834-66-2 <2-(Dimethylaminomethyl)phenyl>-<(6-hydroxy-spiro<4.5>dec-6-yl)methyl>-sulfoxid 
• 73880-57-6 <2-(Dimethylaminomethyl)phenyl>-<(1-hydroxy-3,3,5,5-tetramethylcyclohexyl)methyl>-sulfoxid 
• 73880-60-1 Dimethyl-[2-(3,3,5,5-tetramethyl-cyclohex-1-enylmethanesulfinyl)-benzyl]-amine 
• 73880-59-8 <2-(Dimethylaminomethyl)phenyl>-<(3,3,5,5-tetramethylcyclohexyliden)methyl>-sulfoxid 
• 73880-50-9 <2-(Dimethylaminomethyl)phenyl>-methyl-sulfoxid 
• 344598-93-2 <2-(Dimethylaminomethyl)phenyl>-<(2-trimethylsilyloxybicyclo<2.2.2>oct-2-yl)methyl>-sulfoxid 
• 73880-54-3 <(Bicyclo<2.2.2>oct-2-yliden)methyl>-<2-(dimethylaminomethyl)phenyl>-sulfoxid 
• 73880-55-4 <(Bicyclo<2.2.2>-oct-2-en-2-yl)methyl>-<2-(dimethylaminomethyl)phenyl>-sulfoxid 
• 73880-51-0 <2-(Dimethylaminomethyl)phenyl>-<(2-hydroxybicyclo<2.2.2>oct-2-yl)methyl>-sulfoxid 

Relevant articles and documents

Investigation of the Amide Rotation in N,N-Dialkylbenzamides. 7--Re-examination of the Role of the Hydrogen Bond in 2-Mercapto Substituted Derivatives

Barriers to the amide rotation in mercapto-N,N-dialkylbenzamides and some of their derivatives were measured by dynamic 1H NMR.For N,N-diisopropylamides, barriers to rotation about carbonyl-aryl bond were also determined.The results show that the intramolecular hydrogen bond has only a very small influence on the measured barriers.In contrast to the literature data, only one set of signals, common to all possible forms of 2-mercapto-N,N-dimethylbenzamide, has been observed.