16239-26-2

Basic information

• Product Name: BENZENECARBOXIMIDAMIDE,N-(3-NITROPHENYL)-
• Synonyms: BENZENECARBOXIMIDAMIDE,N-(3-NITROPHENYL)-
• CAS NO: 16239-26-2
• Molecular Formula: C₁₃H₁₁N₃O₂
• Molecular Weight: 241.25
• Mol File: 16239-26-2.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: BENZENECARBOXIMIDAMIDE,N-(3-NITROPHENYL)-(CAS DataBase Reference)
• NIST Chemistry Reference: BENZENECARBOXIMIDAMIDE,N-(3-NITROPHENYL)-(16239-26-2)
• EPA Substance Registry System: BENZENECARBOXIMIDAMIDE,N-(3-NITROPHENYL)-(16239-26-2)

Safety Data

• Hazardous Substances Data: 16239-26-2(Hazardous Substances Data)

Upstream product

• 100-47-0 benzonitrile 
• 99-09-2 3-nitro-aniline 
• 14034-63-0 3-nitroanilinium 4-toluenesulfonate 
• 5341-44-6 N-(3-nitrobenzylidene)aniline 

Downstream Products

• 1350628-98-6 1-(3-nitrophenyl)-2-phenyl-1H-benzo[d]imidazole 
• 43087-91-8 2-phenyl-1,3-benzothiazol-5-amine 
• 4826-10-2 6-nitro-3-phenyl-2H-benzo[e][1,2,4]thiadiazine 1-oxide 
• 4826-02-2 6-nitro-3-phenyl-1-(toluene-4-sulfonylamino)-1λ⁴-benzo[1,2,4]thiadiazine 

Relevant articles and documents

Synthesis and structure of aroylamidines and N-arylbenzamidines hydrochlorides

Aroylamidines can be obtained as salts in a reaction of the corresponding arylcarbonitriles with anhydrous ethanol in the presence of dry HCl followed by treating intermediate imidoesters with alcoholic solution of ammonia. N-Arylbenzamidines are obtained by reacting benzonitrile with arylamines in the presence of AlCl3. The structure of arylamines and the reaction conditions signifi cantly affect the yield of the target product, and sometimes the very possibility of its preparation. Pleiades Publishing, Ltd., 2012.

Reaction of Sulphuryl Chloride with Some Schiff Bases

The reaction of sulphuryl chloride with schiff bases has been studied.In each case, pure crystalline products have been isolated, and their structures elucidated on the basis of IR, PMR and mass spectral data.A plausible mechanism is advanced for the formation of observed products.