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1402146-02-4

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  • Nickel, [6,15-bis(2,4,6-trimethylphenyl)-19,20,21,22-tetraazapentacyclo[14.2.1.12,5.17,10.111,14]docosa-1(19),2,4,6,8,10(21),11,13,15,17-decaenato(2-)-κN19,κN20,κN21,κN22]-, (SP-4-1)-

    Cas No: 1402146-02-4

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1402146-02-4 Usage

General Description

C36H30N4Ni is a chemical compound containing 36 carbon atoms, 30 hydrogen atoms, 4 nitrogen atoms, and 1 nickel atom. It is a complex organonickel compound that is used in various industrial applications and organic synthesis. The presence of the nickel atom in the compound suggests that it may have catalytic or coordinating properties. The exact characteristics and uses of C36H30N4Ni would depend on its specific chemical structure and properties, but it is likely to have a role in reactions involving carbon-carbon and carbon-nitrogen bond formation, as well as potential applications in fields such as pharmaceuticals, agrochemicals, or materials science. Further investigation and analysis would be needed to determine the specific properties and potential uses of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 1402146-02-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,2,1,4 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1402146-02:
(9*1)+(8*4)+(7*0)+(6*2)+(5*1)+(4*4)+(3*6)+(2*0)+(1*2)=94
94 % 10 = 4
So 1402146-02-4 is a valid CAS Registry Number.

1402146-02-4Downstream Products

1402146-02-4Relevant articles and documents

Acid-mediated migration of bromide in an antiaromatic porphyrinoid: Preparation of two regioisomeric Ni(II) bromonorcorroles

Kawashima, Hiroyuki,Hiroto, Satoru,Shinokubo, Hiroshi

, p. 10425 - 10432 (2017)

The regioselective halogenation of porphyrinoids is critical for their selective functionalization, which enables the fine tuning of their electronic and optical properties. Here we report the synthesis of two regioisomeric Ni(II) bromonorcorroles on the

Synthesis and electron-transport properties of a stable antiaromatic NiIInorcorrole with the smallest: Meso -substituent

Fukui, Norihito,Koo, Yun Hee,Seki, Shu,Shinokubo, Hiroshi,Ukai, Shusaku

, p. 14383 - 14387 (2020)

meso-Dimethylnorcorrole NiII complex exhibited enough stability under ambient conditions despite the distinct antiaromaticity. The small methyl substituents realized a dense and long-range π-stacking in its solid state, which resulted in the superior electron-transporting ability to previously reported NiII norcorroles. This journal is

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