134305-63-8 Usage
Uses
Used in Pharmaceutical Industry:
[1,1'-Biphenyl]-4-amine, 4'-methoxy-N,N-bis(4-methoxyphenyl)is used as a building block for the synthesis of pharmaceuticals due to its ability to form new carbon-carbon and carbon-nitrogen bonds. The presence of the amine and methoxy groups allows for the creation of a diverse range of molecular structures with potential therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, [1,1'-Biphenyl]-4-amine, 4'-methoxy-N,N-bis(4-methoxyphenyl)is used as a key component in the development of new agrochemicals. Its versatile reactivity and structural features contribute to the design and synthesis of compounds with targeted biological activities, such as pesticides and herbicides.
Used in Materials Science:
[1,1'-Biphenyl]-4-amine, 4'-methoxy-N,N-bis(4-methoxyphenyl)is also used in materials science for the development of novel materials with specific properties. [1,1'-Biphenyl]-4-amine, 4'-methoxy-N,N-bis(4-methoxyphenyl)-'s structural features and functional groups can be exploited to create materials with tailored characteristics for various applications, such as in electronics, coatings, or advanced composites.
Used in Organic Chemistry Research:
As a versatile reagent, [1,1'-Biphenyl]-4-amine, 4'-methoxy-N,N-bis(4-methoxyphenyl)is used in organic chemistry research for the exploration of new reaction pathways and the synthesis of complex molecular structures. Its unique properties make it an invaluable tool for chemists working on the development of new compounds and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 134305-63-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,3,0 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 134305-63:
(8*1)+(7*3)+(6*4)+(5*3)+(4*0)+(3*5)+(2*6)+(1*3)=98
98 % 10 = 8
So 134305-63-8 is a valid CAS Registry Number.
134305-63-8Relevant academic research and scientific papers
Electron-transfer process in layered photoreceptors containing azo compounds
Shimada, Tomoyuki,Sasaki, Masaomi,Aruga, Tamotsu,Umeda, Minoru
, p. 785 - 793 (2007/10/03)
Photoinduced electron transfer (ET) is the most essential process for carrier photogeneration in organic optoelectronic devices. In azo compound- based layered photoreceptors, carrier photogeneration is sensitized by hole transport material (HTM) incorporation. We investigated this process to elucidate the highly sensitizing mechanism. First, the photoinduced ET efficiency and overall quantum efficiency were measured and compared for the layered photoreceptor and the carrier generation layer. The result that the HTM enhances the photoinduced ET implies that the HTM works catalytically to diminish the activation energy. Although such extrinsic ET takes place independently of an electric field, the subsequent geminate pair dissociation depends on the electric field. Next, the energy-gap dependence of the ET was investigated by employing more than 50 photoreceptors to vary the energy gap over a wide range. The measured efficiency was plotted against the energy gap, in which an inverted region was not observed.
