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1285686-72-7

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1285686-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1285686-72-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,5,6,8 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1285686-72:
(9*1)+(8*2)+(7*8)+(6*5)+(5*6)+(4*8)+(3*6)+(2*7)+(1*2)=207
207 % 10 = 7
So 1285686-72-7 is a valid CAS Registry Number.

1285686-72-7Downstream Products

1285686-72-7Relevant academic research and scientific papers

Triphenylamine-modified difluoroboron dibenzoylmethane derivatives: Synthesis, photophysical and electrochemical properties

Zhang, Hao,Liu, Chun,Xiu, Jinghai,Qiu, Jieshan

, p. 798 - 806 (2017)

Two new triphenylamine functionalized difluoroboron (BF2) β-diketonate complexes, one asymmetrical 2 and the other symmetrical 3, were synthesized and fully characterized. The effects of the triphenylamine substituent on the photoluminescence,

Preparation method of triphenylamine-containing platinum complex and oxygen sensing application of complex

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Paragraph 0015, (2018/04/03)

The invention relates to a preparation method of a beta-diketone auxiliary ligand-platinum complex and oxygen sensing application of the complex, belonging to the technical field of luminescent materials. The complex is formed by 2-phenylpyridine C^N type cycle metal ligand and a beta-diketone auxiliary ligand synthesized by parabromoacetophenone, methyl benzoate and 4-triphenylamine boric acid with platinum metal ions through common complexation. The platinum complex has good oxygen sensing performance and further has reversible phosphorescence quenching and recovery processes. An oxygen sensor prepared from the platinum complex can be used for monitoring oxygen concentration on line.

Synthesis of triphenylamine-modified arylates and ketones via suzuki coupling reactions

Wang, Jian,Yang, Chang-Jian,Peng, Hua-Nan,Deng, Yang-Sheng,Gao, Xi-Cun

, p. 832 - 840 (2011/04/22)

A series of triphenylamine-mdified arylates and ketones were synthesized via Pd-catalyzed Suzuki coupling reaction of triphenylamine boronic acid with aryl bromide. The triphenylamine boronic acid was synthesized by iodization of 4-bromoaniline, Ullmann reaction of 1-bromo-4-iodobenzene with diphenylamine, and boronic acidification of 4-bromotriphenylamine.

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