4810-30-4 Usage
Uses
Used in Pharmaceutical Industry:
[1,1'-Biphenyl]-2-amine, 4,4'-dichlorois used as a building block for the development of pharmaceutical compounds due to its potential applications in drug development and research purposes. Its unique structure allows for the creation of various derivatives and analogs that can be tailored for specific therapeutic uses.
Used in Agrochemical Industry:
In the agrochemical industry, [1,1'-Biphenyl]-2-amine, 4,4'-dichlorois used as a starting material for the synthesis of agrochemicals, such as pesticides and herbicides. Its reactivity and structural properties make it a suitable candidate for the development of new and effective compounds in this field.
Used in Materials Science:
[1,1'-Biphenyl]-2-amine, 4,4'-dichlorois also utilized in materials science for the development of novel materials with specific properties. Its unique structure and reactivity can contribute to the creation of advanced materials with potential applications in various industries.
Safety Precautions:
Proper handling and safety precautions should be followed when working with [1,1'-Biphenyl]-2-amine, 4,4'-dichlorodue to its potential hazards. It is essential to adhere to safety guidelines and protocols to minimize risks associated with this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 4810-30-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,1 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4810-30:
(6*4)+(5*8)+(4*1)+(3*0)+(2*3)+(1*0)=74
74 % 10 = 4
So 4810-30-4 is a valid CAS Registry Number.
4810-30-4Relevant academic research and scientific papers
Zhu, Chendan,Wang, Di,Wang, Dingyi,Zhao, Yue,Sun, Wei-Yin,Shi, Zhuangzhi
, p. 8848 - 8853 (2018)
A straightforward method was developed for construction of aromatic compounds with a triphenylene core. The method involves Pd-catalyzed annulative dimerization of o-iodobiaryl compounds by double C?I and C?H bond cleavage steps. Simple reaction conditions are needed, requiring neither a ligand nor an oxidant, and the reaction tolerates a wide range of coupling partners without compromising efficiency or scalability. Significantly, the tetrachloro-substituted synthon, 1,6,11-trichloro-4-(4-chlorophenyl)triphenylene, can be generated and used to prepare a series of fully fused, small graphene nanoribbons by a late-stage arylation with arylboronic acids and a subsequent Scholl reaction. The synthetic strategy enables bottom-up access to extended π-systems in a controlled manner.
