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1,2,4-Triazine, 3-(4-bromophenyl)-6-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66600-10-0

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66600-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66600-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,6,0 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 66600-10:
(7*6)+(6*6)+(5*6)+(4*0)+(3*0)+(2*1)+(1*0)=110
110 % 10 = 0
So 66600-10-0 is a valid CAS Registry Number.

66600-10-0Downstream Products

66600-10-0Relevant academic research and scientific papers

Metatriazine compound and electronic device

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Paragraph 0125-0129, (2020/09/23)

The invention relates to a metatriazine compound and an electronic device. By introducing a metatriazine rigid structure, the metatriazine compound provided by the invention has excellent film-formingproperty and thermal stability, and can be used for preparing organic electroluminescent devices, organic field effect transistors and organic solar cells. In addition, the metatriazine compound canbe used as a constituent material of a hole injection layer, a hole transport layer, a light emitting layer, an electron blocking layer, a hole blocking layer or an electron transport layer, and can reduce the driving voltage, improve the efficiency, improve the brightness, prolong the service life and the like. In addition, the metatriazine compound is simple in preparation method, raw materialsare easy to obtain, and the industrial development requirement can be met.

One-Pot Acid-Catalyzed Ring-Opening/Cyclization/Oxidation of Aziridines with N-Tosylhydrazones: Access to 1,2,4-Triazines

Crespin, Lorène,Biancalana, Lorenzo,Morack, Tobias,Blakemore, David C.,Ley, Steven V.

, p. 1084 - 1087 (2017/03/15)

A new, three-step, telescoped reaction sequence for the regioselective conversion of N-tosyl hydrazones and aziridines to 3,6-disubstituted and 3,5,6-trisubstituted 1,2,4-triazines is described. The process involves an efficient nucleophilic ring opening of the aziridine, giving access to a wide range of aminohydrazones, isolated with excellent yields. A “one-pot” procedure, combining the ring opening with a cyclization and an oxidation step, allows the preparation of diversified triazines in good yields.

Synthesis of 6-Substituted 3,5-diaryl-1,2,4-triazines as Potential Herbicidal Agents

Konno, Shoetsu,Osawa, Noriko,Yamanaka, Hiroshi,Sanemitsu, Yuzuru,Kawamura, Shinichi,Sakaki, Masaharu

, p. 838 - 842 (2007/10/02)

A variety of 6-substituted 3,5-diaryl-1,2,4-triazines were synthesized.These diaryltriazines, which incorporate a triazine nucleus substituted by two aryl moietes, comprise a new class of bleaching herbicides.The structure-activity relationships were prov

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