19732-23-1

Basic information

• Product Name: 4,N-dimethyl-6-(N-methyl-p-toluidinomethyl)aniline
• Synonyms: 4,N-dimethyl-6-(N-methyl-p-toluidinomethyl)aniline
• CAS NO: 19732-23-1
• Molecular Weight: 254.375
• Mol File: 19732-23-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4,N-dimethyl-6-(N-methyl-p-toluidinomethyl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 4,N-dimethyl-6-(N-methyl-p-toluidinomethyl)aniline(19732-23-1)
• EPA Substance Registry System: 4,N-dimethyl-6-(N-methyl-p-toluidinomethyl)aniline(19732-23-1)

Safety Data

• Hazardous Substances Data: 19732-23-1(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 623-08-5 N-methyl-p-toluidine 
• 7137-82-8 N,N'-dimethyl-N,N'-di-p-tolylmethanediamine 
• 99-97-8 Dimethyl-p-toluidine 
• 97188-69-7 bis<2-(N-methyltrifluoroacetamido)-5-methylphenyl>methane 
• 38151-54-1 6-chloro-5,6,7,12-tetrahydro-2,5,7,10-tetramethyldibenzo<1,3,2>-diazaphosphocine 6-sulphide 
• 19732-22-0 6-chloro-5,6,7,12-tetrahydro-2,5,7,10-tetramethyldibenzo<1,3,2>diazaphosphocine 6-oxide 
• 114660-21-8 2,2'-methylenebis(N-acetyl-N-methyl-p-toluidine) 
• 17293-74-2 4,N-dimethyl-6-(N-methyl-p-toluidinomethyl)aniline 

Relevant articles and documents

Phosphorus-Nitrogen Compounds. Part 49. The Synthesis and Mechanism of Formation of 6-Chloro-5,6,7,12-tetrahydro-2,5,7,10-tetramethyldibenzo-diazaphosphocine 6-Oxide and 6-Sulphide

A reaction mechanism is proposed for the formation of the title compounds in the reactions between N,N-dimethyl-p-toluidine and phosphoryl and thiophosphoryl chlorides.The synthesis of 2,2'-methylenebis(p-toluidine) and 2,2'-methylenebis(N-methyl-p-toluidine) are described, as are their reactions with phosphoryl and thiophosphoryl chlorides.

The preparation of some fused isothiazole derivatives

The treatment of di(2-amino-5-methylphenyl)methane with N-sulfinylmethanesulfonamide gives two materials, 3-(2-amino-5-methylphenyl)-5-methyl-2,1-benzisothiazole and what appears to be its tautomer, a 2,1-benzisothiazolo-2,1-benzisothiazole derivative.Reaction of the former with methyl iodide gives mono-, di-, and trimethyl derivatives.The second of these also possesses the symmetrical 2,1-benzisothiazolo-2,1-benzisothiazole structure.The structure of the other methylation product and of the acetylation products are discussed.Some 1,2-dithiol-3-ylidene-2-pyridylmethanes were made by condensation of 3-alkylthio-1,2-dithiolium salts with methyl 2-pyridylacetate.These demonstrate little sulfur-nitrogen interaction. 3-Methylthio-4-phenyl-1,2-dithiolium iodide reacts anomalously with methyl 2-pyridylacetate to form a quinolizinethione. 1,2-Benzisothiazolopyridinium triiodide was made by iodine oxidation of 2-(2-mercaptophenylpyridine).