57609-72-0 Usage
Uses
Used in Pharmaceutical Industry:
4-[2-[5-[4-(Diethylamino)phenyl]-4,5-dihydro-1-phenyl-1H-pyrazol-3-yl]vinyl]-N,N-diethylaniline is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique structure allows for the development of new compounds with potential therapeutic effects, particularly in the treatment of diseases that require novel drug targets.
Used in Organic Synthesis:
In the field of organic synthesis, 4-[2-[5-[4-(Diethylamino)phenyl]-4,5-dihydro-1-phenyl-1H-pyrazol-3-yl]vinyl]-N,N-diethylaniline serves as a key building block for the creation of more complex organic molecules. Its versatile functional groups enable it to participate in a wide range of chemical reactions, facilitating the synthesis of new compounds with diverse applications.
Used in Material Sciences:
4-[2-[5-[4-(Diethylamino)phenyl]-4,5-dihydro-1-phenyl-1H-pyrazol-3-yl]vinyl]-N,N-diethylaniline is utilized in material sciences for the development of advanced materials with specific properties. Its highly conjugated structure and functional groups can contribute to the creation of materials with unique optical, electronic, or mechanical characteristics, suitable for various high-tech applications.
Check Digit Verification of cas no
The CAS Registry Mumber 57609-72-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,6,0 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 57609-72:
(7*5)+(6*7)+(5*6)+(4*0)+(3*9)+(2*7)+(1*2)=150
150 % 10 = 0
So 57609-72-0 is a valid CAS Registry Number.
InChI:InChI=1/C31H38N4/c1-5-33(6-2)28-20-15-25(16-21-28)14-19-27-24-31(35(32-27)30-12-10-9-11-13-30)26-17-22-29(23-18-26)34(7-3)8-4/h9-23,31H,5-8,24H2,1-4H3/b19-14-
57609-72-0Relevant academic research and scientific papers
Electrophotographic member
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, (2008/06/13)
Disclosed is an electrophotographic member containing as a charge transport material a fluorine-containing N,N,N',N'-tetraarylbenzidine derivative which is remarkably excellent in solubility in an organic solvent and/or a binder such as polycarbonate resin, etc., can show very excellent electrophotographic properties such as high sensitivity, low residual potential and high durability. Further, a fluorine-containing N,N,N',N'-tetraarylbenzidine derivative usable as a charge transport material, and a process for producing the same are disclosed. Furthermore, a fluorine-containing diarylamine usable for producing the fluorine-containing N,N,N',N'-tetraarylbenzidine derivative, and a process for producing the same are disclosed.
REACTION OF SINGLET OXYGEN WITH 2-PYRAZOLINE: IMPLICATION FOR CATION RADICAL - SUPEROXIDE ION PAIR INTERMEDIATE
Akasaka, Takeshi,Nakagawa, Masaru,Nomura, Yuko,Sato, Rikiya,Someno, Kazuo,Ando, Wataru
, p. 3807 - 3812 (2007/10/02)
Kinetic studies on photosensitized oxygenation of 1,3,5-triaryl-2-pyrazolines show that an electron-transfer from the pyrazoline to singlet oxygen may take place to give a cation radical and superoxide ion pair.The reaction of pyrazoline cation radicals with superoxide ion shows the same product distribution with singlet oxygenation.
