553-74-2

Usage

Uses

Used in Analytical Chemistry:
Anthranilaldehyde phenylhydrazone is used as a reagent for the detection of nitrites and colibacilli in urine. This application is based on its ability to form colored complexes with these substances, which can be easily detected and quantified using spectrophotometric methods. anthranilaldehyde phenylhydrazone has been cited in the literature for its use in this context, as referenced in Pfeiffer, Muench. Med. Wochenschr. 92, 1315 (1950).
Additionally, anthranilaldehyde phenylhydrazone may have other applications in different industries, such as:
Used in Pharmaceutical Industry:
Anthranilaldehyde phenylhydrazone can be used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows it to be a versatile building block for the development of new drugs with potential therapeutic applications.
Used in Chemical Synthesis:
In the field of organic chemistry, anthranilaldehyde phenylhydrazone can be employed as a synthetic intermediate for the preparation of a wide range of organic compounds, including dyes, pigments, and other specialty chemicals.
Used in Research and Development:
Anthranilaldehyde phenylhydrazone may also be utilized in research and development settings to study the properties and reactivity of hydrazone derivatives, as well as to explore new synthetic routes and methodologies for the preparation of complex organic molecules.

InChI:InChI=1/C13H13N3/c14-13-9-5-4-6-11(13)10-15-16-12-7-2-1-3-8-12/h1-10,16H,14H2

Upstream product

• 271-58-9 anthranil 
• 100-63-0 phenylhydrazine 
• 102174-89-0 3,9-bis-(2-nitro-phenyl)-2,4,8,10-tetraoxa-spiro[5.5]undecane 
• 110-86-1 pyridine 
• 25334-63-8 10,11-dihydro-5aH,17H-5,11-cyclo-dibenzo[3,4;7,8][1,5]diazocino[2,1-b]quinazolin-17-ol 
• 5435-44-9 (E)-3-Ureido-but-2-enoic acid ethyl ester 
• 64-19-7 acetic acid 
• 529-23-7 o-aminobenzaldehyde 
• 16004-43-6 o-nitrobenzaldehyde semicarbazone 
• 552-89-6 2-nitro-benzaldehyde 
• 610-64-0 1-(2-nitrobenzylidene)-2-phenylhydrazine 
• 271-61-4 benzo[c]isothiazole 
• 876-92-6 2-phenyl-2,4-dihydro-pyrazol-3-one 
• 7732-18-5 water 

Relevant academic research and scientific papers

Synthesis, spectroscopic, thermal, and photostability studies of 2-aminobenzaldehyde phenylhydrazone (2ABPH) as fluorescent dye and their Cu(II), Co(II), and Mn(II) complexes

Herein, the 2-aminobenzaldehyde phenylhydrazone (2ABPH) Schiff base and their mononuclear Mn(II), Co(II), and Cu(II) complexes were reported. The structures of the complexes have been elucidated by elemental analysis, molar conductivity, magnetic properties, infrared, electronic, mass spectra, and thermal studies. The stoichiometries of the 2ABPH complexes accordance of the mentioned analysis give the general formula [M(2ABPH)2(Cl) 2]·xH2O (where M is Mn(II), Co(II), Cu(II), and x = 1, 4 and 6). The photo stabilities of the Schiff base and their complexes were examined. Copyright Taylor & Francis Group, LLC.

Synthesis, infrared spectra and thermal studies of Zn(II), Cd(II) and Hg(II) complexes with 2-aminobenzaldehyde phenylhydrazone "nitrin" ligand

The, nitrin, 2-aminobenzaldehyde phenylhydrazone (2ABPH) was synthesis by refluxing 2-nitrobenzaldehyde with phenylhydrazine in ethanolic solvent. Three transition metal (II) complexes of 2ABPH have been prepared. Elemental analysis, molar conductivity, IR, UV, 1H NMR, and mass spectra, as well as TG/DTG have been used to characterize these complexes. The complexes have the general formula [M(2ABPH)2]Cl2·nH2O, where M = Zn, Cd, and Hg and n = 4, 2 and 0 for Zn(II), Cd(II) and Hg(II), respectively. The ligand and its complexes have been studied for their possible biological activity including antibacterial and antifungal activity.

Friedlaender Condensation of 1H-Pyrazolin-5-ones with o-Aminobenzaldehydes. Synthesis of 1H-Pyrazoloquinolines

All the possible 1- and 3-monomethyl, monophenyl, dimethyl, diphenyl, and methylphenyl-1H-pyrazolin-5-ones have been condensed with o-aminobenzaldehyde.In some cases (but not all) 1-H-pyrazoloquinolines (10) are formed together with a variety of other products.The balance between formation of hydrazone 11 and the ring-closed 10 is discussed, as is the formation of other products obtained in these condensations.