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4-chloro-2,3-diphenyl-1H-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81303-08-4

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81303-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81303-08-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,3,0 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 81303-08:
(7*8)+(6*1)+(5*3)+(4*0)+(3*3)+(2*0)+(1*8)=94
94 % 10 = 4
So 81303-08-4 is a valid CAS Registry Number.

81303-08-4Relevant academic research and scientific papers

ORGANIC ELECTROLUMINESCENCE DEVICE AND AMINE COMPOUND FOR ORGANIC ELECTROLUMINESCENCE DEVICE

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Paragraph 0362-0363; 0364-0365, (2020/04/17)

An organic electroluminescence device according to embodiments of the present disclosure includes a first electrode, a second electrode opposite the first electrode, and at least one organic layer between the first electrode and the second electrode, wherein the at least one organic layer includes an amine compound represented by Formula 1, and HT in Formula 1 includes a pyridoindole moiety represented by Formula 2. Improved device efficiency and life characteristics may be achieved when the amine compound represented by Formula 1 is included in the organic electroluminescence device.

A kind of high-efficient synthetic indole and isoquinoline derivatives (by machine translation)

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Paragraph 0041; 0042, (2016/10/07)

The invention discloses a substituted indole and isoquinoline preparation method, which belongs to the technical field of organic chemical synthesis. This method adopts the oxygen as the oxidizing agent, various substituents substituted alkyne starting material of the aromatic amine or [...] , by transition metal-catalyzed, get containing indole or isoquinoline compound of the structure. The reaction raw material, oxidizing agent and cheap and easily obtained catalyst, synthesis technique is simple, which greatly reduces the cost of synthesizing; mild reaction conditions, high yield, easy industrialization; reaction raw materials and catalyst cleaning non-toxic, small pollution to the environment. Such compounds and their derivatives as an important fine chemicals, in the medical, agricultural chemicals, perfume and widely used photoelectric and other industries. (by machine translation)

Rh-Catalyzed oxidative C-H activation/annulation: Converting anilines to indoles using molecular oxygen as the sole oxidant

Zhang, Guoying,Yu, Hui,Qin, Guiping,Huang, Hanmin

supporting information, p. 4331 - 4334 (2014/04/17)

A practical and efficient Rh(iii)-catalyzed aerobic C-H activation has been developed for the facile synthesis of a broad range of indoles from simple anilines and alkynes. The protocol could be conducted under mild conditions and used environmentally friendly oxygen as the sole clear oxidant.

SUBSTITUENT INFLUENCE ON THE INDOLIZATION WITH PCl3 OF SOME o,m,p-SUBSTITUTED PHENYLHYDRAZONES

Baccolini, Graziano,Marotta, Emanuela

, p. 4615 - 4620 (2007/10/02)

The indolization of deoxybenzoin o,m,p (Me, MeO, Cl), p-NO2 and m-EtO-phenylhydrazones (1) by the above reaction has been examined.All the reactions are carried out at room temperature and high yields of the corresponding indoles (2) are obtained even whe

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