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4,4'-Dichloro-2-iodobiphenyl is a synthetic organic compound characterized by its chemical formula C12H7Cl2I. It is a halogenated derivative of biphenyl, with two chlorine atoms attached to the 4 and 4' positions and an iodine atom at the 2 position. 4,4’-dichloro-2-iodobiphenyl is typically used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its halogenated nature, it may exhibit certain environmental and health concerns, such as potential toxicity and persistence in the environment. As a result, its production, use, and disposal are subject to strict regulations to minimize any adverse effects on human health and the ecosystem.

4510-80-9

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4510-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4510-80-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,1 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4510-80:
(6*4)+(5*5)+(4*1)+(3*0)+(2*8)+(1*0)=69
69 % 10 = 9
So 4510-80-9 is a valid CAS Registry Number.

4510-80-9Upstream product

4510-80-9Relevant academic research and scientific papers

Bottom-up Construction of π-Extended Arenes by a Palladium-Catalyzed Annulative Dimerization of o-Iodobiaryl Compounds

Zhu, Chendan,Wang, Di,Wang, Dingyi,Zhao, Yue,Sun, Wei-Yin,Shi, Zhuangzhi

, p. 8848 - 8853 (2018/05/08)

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.

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