553-74-2 Usage
Description
Anthranilaldehyde phenylhydrazone is an organic compound that is formed through the reaction between anthranilaldehyde and phenylhydrazine. It is a derivative of hydrazone, which is a class of organic compounds that are characterized by the presence of a hydrazone functional group. Anthranilaldehyde phenylhydrazone is known for its analytical and synthetic applications in various fields.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 553-74-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,5 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 553-74:
(5*5)+(4*5)+(3*3)+(2*7)+(1*4)=72
72 % 10 = 2
So 553-74-2 is a valid CAS Registry Number.
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
553-74-2Relevant articles and documents
Synthesis, spectroscopic, thermal, and photostability studies of 2-aminobenzaldehyde phenylhydrazone (2ABPH) as fluorescent dye and their Cu(II), Co(II), and Mn(II) complexes
Refat, Moamen S.,Killa, Hamada M.A.,Mansour, Asmaa F.,Fetooh, Hammad
, p. 295 - 308 (2011)
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.
Friedlaender Condensation of 1H-Pyrazolin-5-ones with o-Aminobenzaldehydes. Synthesis of 1H-Pyrazoloquinolines
Tomasik, Danuta,Tomasik, Piotr,Abramovitch, Rudolph A.
, p. 1539 - 1543 (2007/10/02)
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.
