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2-([1,1'-biphenyl]-3-yln)aphthalene is an organic compound characterized by a naphthalene molecule with a biphenyl group attached at the 2-position. 2-([1,1'-biphenyl]-3-yl)naphthalene consists of a naphthalene ring, which is a fused pair of benzene rings, and a biphenyl group, which is essentially two benzene rings connected by a single bond. The specific arrangement of these rings in 2-([1,1'-biphenyl]-3-yl)naphthalene results in a unique molecular structure that can influence its chemical properties and potential applications. The compound may be of interest in various fields, including materials science and organic chemistry, due to its distinct structure and the possibility of it exhibiting specific electronic or optical properties.

87294-80-2

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87294-80-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87294-80-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,9 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87294-80:
(7*8)+(6*7)+(5*2)+(4*9)+(3*4)+(2*8)+(1*0)=172
172 % 10 = 2
So 87294-80-2 is a valid CAS Registry Number.

87294-80-2Downstream Products

87294-80-2Relevant academic research and scientific papers

Ni-Catalyzed Cross-Coupling of Dimethyl Aryl Amines with Arylboronic Esters under Reductive Conditions

Cao, Zhi-Chao,Xie, Si-Jun,Fang, Huayi,Shi, Zhang-Jie

, p. 13575 - 13579 (2018)

Herein, we reported a successful Suzuki-Miyaura coupling of dimethyl aryl amines to forge biaryl skeleton via Ni catalysis in the absence of directing groups and preactivation. This transformation proceeded with high efficiency in the presence of magnesium. Preliminary mechanism studies demonstrated dual roles of magnesium: (i) a reductant that reduced Ni(II) species to active Ni(I) catalyst; (ii) a unique promoter that facilitated the Ni(I)/Ni(III) catalytic cycle.

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