951-48-4

Basic information

• Product Name: BENZENECARBOXIMIDAMIDE,2-AMINO-N-PHENYL-
• Synonyms: BENZENECARBOXIMIDAMIDE,2-AMINO-N-PHENYL-
• CAS NO: 951-48-4
• Molecular Formula: C₁₃H₁₃N₃
• Molecular Weight: 211.26
• Mol File: 951-48-4.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• CAS DataBase Reference: BENZENECARBOXIMIDAMIDE,2-AMINO-N-PHENYL-(CAS DataBase Reference)
• NIST Chemistry Reference: BENZENECARBOXIMIDAMIDE,2-AMINO-N-PHENYL-(951-48-4)
• EPA Substance Registry System: BENZENECARBOXIMIDAMIDE,2-AMINO-N-PHENYL-(951-48-4)

Safety Data

• Hazardous Substances Data: 951-48-4(Hazardous Substances Data)

Upstream product

• 62-53-3 aniline 
• 1885-29-6 anthranilic acid nitrile 

Downstream Products

• 34923-95-0 4-(phenylamino)quinazoline 
• 324521-72-4 [2-(4-chloro-phenyl)-2,3-dihydro-1H-quinazolin-4-ylidene]-phenyl-amine 
• 324521-65-5 phenyl-(2-phenyl-2,3-dihydro-1H-quinazolin-4-ylidene)-amine 
• 324521-73-5 [2-(4-bromo-phenyl)-2,3-dihydro-1H-quinazolin-4-ylidene]-phenyl-amine 
• 324521-66-6 phenyl-(2-m-tolyl-2,3-dihydro-1H-quinazolin-4-ylidene)-amine 
• 1015164-91-6 C₂₁H₂₁N₃O₆ 
• 1015164-92-7 C₂₉H₂₁N₃O₆ 
• 1015164-91-6 N',N''-bis(3-carboxy-1-oxopropanyl) 2-amino-N-arylbenzamidine 
• 1015164-92-7 N',N''-bis(3-carboxy-1-oxophenelenyl) 2-amino-N-arylbenzamidine 
• 1262424-46-3 (Z)-N-(2-p-tolyl-2,3-dihydroquinazolin-4(1H)-ylidene)aniline 
• 1262424-51-0 (Z)-N-(2-(naphthalen-1-yl)-2,3-dihydroquinazolin-4(1H)-ylidene)aniline 
• 67461-76-1 2-oxo-3-phenyl-4-imino-1,2,3,4-tetrahydroquinazoline 
• 603-23-6 3-phenyl-2,4-(1H,3H)-quinazolinedione 
• 731-51-1 4-oxo-3-phenyl-3,4-dihydroquinazoline-2-carbonitrile 

Relevant articles and documents

Synthesis of novel quinazolines via nucleophilic cycloaddition of 2-amino-N′-arylbenzimidamides with dimethyl acetylenedicarboxylate and 2-(dicyanomethylene)indan-1,3-dione

Abstract: Synthesis of novel tetrahydroquinazoline-2-carboxylate and arylaminoquinazoline-2-carboxylate in good yields has been established via the nucleophilic cycloaddition of 2-amino-N′-arylbenzimidamides on dimethyl acetylenedicarboxylate. Moreover, studying the reaction of 2-amino-N′-arylbenzimidamides with 2-(dicyanomethylene)indan-1,3-dione to give 3,4-dihydroquinazolin derivatives. The results obtained from IR, 1H NMR, and 13C NMR data as well as the mass spectra are in agreement with the assigned structures. A plausible mechanism for the formation of the products is presented. Graphic abstract: [Figure not available: see fulltext.].

Synthesis of 1,3,2-Benzodiazaphosphorine and 1,3,2-Benzodiazaphosphorine-2-sulfide

Background: Benzodiazaphosphorines have many biological activities such as fungicidal and antitumor. In this work we are interested to synthesize them in order to test their activities in future work. The probable mechanism of obtained benzodiazaphosphorines is discussed. Methods: The obtained benzodiazaphosphorines were characterized using FT-IR, NMR 1H and 13C spectroscopy and elemental analysis. Results: A series of new benzodiazaphosphorines products synthesized were purified by crystallization and obtained with good yields. Conclusion: In this paper we have synthesized a series of benzodiazaphosphorine and benzodiazaphosphorine sulfide which are identified using FT-IR, NMR spectroscopy and elemental analysis. The prepared compounds will be subsequently studied in order to tested their biological activities.

The first indazolimine-arylazobenzonitrile rearrangement

A series of 2-arylazobenzonitriles (5a-f) have been obtained through a novel indazolimine-arylazobenzonitrile rearrangement. The products 5a-f were fully characterized and their structure elucidated on the basis of spectroscopic and analytical data. The mechanism of formation of 5a-f is discussed.