4231-31-6

Basic information

• Product Name: Benzenamine, N-ethynyl-N-methyl-
• CAS NO: 4231-31-6
• Molecular Formula: C9H9N
• Molecular Weight: 131.177
• Mol File: 4231-31-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 83 °C(Press: 10 Torr)
• Density: 1.027±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Benzenamine, N-ethynyl-N-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N-ethynyl-N-methyl-(4231-31-6)
• EPA Substance Registry System: Benzenamine, N-ethynyl-N-methyl-(4231-31-6)

Safety Data

• Hazardous Substances Data: 4231-31-6(Hazardous Substances Data)

Upstream product

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Downstream Products

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• 115943-69-6 1-(Methylphenylamino)-4,4-bis(phenylsulfonyl)-1-cyclobuten 
• 131497-51-3 Methyl-(4-oxo-2-p-tolyl-4H-4λ⁴-[1,4,3]oxathiazin-6-yl)-phenyl-amine 
• 84274-95-3 1-1,N¹-Dimethyl-N²-(p-tosyl)amidino>-5--1,2,3-triazol 
• 92177-77-0 3-(Dimethylphenylsilyl)-N-methyl-2,3-butadienanilid 
• 120229-79-0 2-<1-(2-Hhydroxy-4,4-dimethyl-6-oxo-1-cyclohexen-1-yl)-cyclopropyl>-N-methyl-N-phenylacetamid 
• 86289-41-0 2-[(Z)-3-(Methyl-phenyl-amino)-3-(4-methyl-[1,2,3]triazol-2-yl)-allylidene]-malononitrile 
• 86289-44-3 2-[(E)-1-(Methyl-phenyl-amino)-3-(4-methyl-[1,2,3]triazol-1-yl)-allylidene]-malononitrile 
• 84274-96-4 1-2-(4-Chlorphenylsulfonyl)-N¹,N¹-dimethylamidino>-5--1,2,3-triazol 
• 86289-43-2 2-[(Z)-3-(4-Methoxy-[1,2,3]triazol-2-yl)-3-(methyl-phenyl-amino)-allylidene]-malononitrile 
• 86289-45-4 2-[(E)-3-(5-Methoxy-[1,2,3]triazol-1-yl)-1-(methyl-phenyl-amino)-allylidene]-malononitrile 

Relevant articles and documents

Triphenylbismuth Dichloride-Mediated Conversion of Thioamides to Nitriles

Thioamides were efficiently converted to nitriles using the pentavalent triphenylbismuth dichloride in combination with triethylamine. The reaction involved the dehydrosulfurization of primary thioamides to afford substituted aromatic or aliphatic nitriles in good to excellent yields. The process was also successfully extended to the synthesis of cyanamides starting from the corresponding thioureas and of thiocyanates from dithiocarbamates.