337498-40-5 Usage
Uses
Used in Organic Synthesis:
1(2H)-Phthalazinone, 2-[5-(4-morpholinyl)-2-nitrophenyl]-4-phenylis utilized as a reagent in organic synthesis, where its distinct structure and functional groups facilitate the creation of a wide range of organic compounds. The presence of the nitrophenyl and phenyl groups allows for further chemical modifications, enhancing the compound's versatility in synthetic applications.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 1(2H)-Phthalazinone, 2-[5-(4-morpholinyl)-2-nitrophenyl]-4-phenylserves as a valuable building block for the synthesis of various drugs. Its unique structure and functional groups make it a promising candidate for the development of new therapeutic agents, potentially targeting a range of medical conditions.
Used in Agrochemicals:
1(2H)-Phthalazinone, 2-[5-(4-morpholinyl)-2-nitrophenyl]-4-phenylis also employed in the agrochemical sector, where its structural features and functional groups can be harnessed to develop novel compounds with applications in pest control, crop protection, and other agricultural practices.
Used in Materials Science:
1(2H)-Phthalazinone, 2-[5-(4-morpholinyl)-2-nitrophenyl]-4-phenyl-'s structural diversity and functional group versatility make it a valuable asset in materials science. 1(2H)-Phthalazinone, 2-[5-(4-morpholinyl)-2-nitrophenyl]-4-phenylcan be used to develop new materials with specific properties, such as improved mechanical strength, thermal stability, or chemical resistance, depending on the desired application.
Check Digit Verification of cas no
The CAS Registry Mumber 337498-40-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,7,4,9 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 337498-40:
(8*3)+(7*3)+(6*7)+(5*4)+(4*9)+(3*8)+(2*4)+(1*0)=175
175 % 10 = 5
So 337498-40-5 is a valid CAS Registry Number.
337498-40-5Relevant academic research and scientific papers
Efficient route to benzo[4,5]imidazo[2,1-a]phthalazines
Kuznetsov, Viktor A.,Shubin, Kirill M.,Schipalkin, Andrej A.,Petrov, Mikhail L.
, p. 10018 - 10030 (2007/10/03)
Benzo[4,5]imidazo[2,1-a]phthalazines have been obtained from various o-nitrophenylhydrazines through different 2-(2-nitrophenyl)-1,2-dihydro-1-phthalazinones as intermediates using an elaborated advanced procedure. An activated chlorine atom in 2-nitrophe
Synthesis of benzo[4,5]imidazo[2,1-a]phthalazines
Shubin, Kirill M.,Kuznetsov, Viktor A.,Galishev, Vladimir A.
, p. 1407 - 1408 (2007/10/03)
5,9-Disubstituted benzo[4,5]imidazo[2,1-a]phthalazines are synthesized efficiently from acylbenzoic acids and 2-nitro-5-chlorophenylhydrazine. Nucleophilic substitution in phthalazinones gave a variety of the title compounds after reduction and cyclizatio
