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3-CHLORO-5,6-DIPHENYL-1,2,4-TRIAZINE is a chemical compound that belongs to the class of triazines. It is characterized by a central triazine ring with three nitrogen atoms and three phenyl groups attached to it, along with a chlorine atom. This white to off-white crystalline powder is primarily used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes.

34177-11-2

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34177-11-2 Usage

Uses

Used in Pharmaceutical Industry:
3-CHLORO-5,6-DIPHENYL-1,2,4-TRIAZINE is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
3-CHLORO-5,6-DIPHENYL-1,2,4-TRIAZINE is used as a precursor in the production of agrochemicals, specifically as a herbicide, insecticide, and fungicide. Its ability to inhibit the growth of unwanted plants and pests makes it a valuable component in agricultural applications.
Used in Dye Industry:
3-CHLORO-5,6-DIPHENYL-1,2,4-TRIAZINE is utilized as an intermediate in the synthesis of dyes, playing a role in the creation of colorants for various industries such as textiles, plastics, and printing.
It is crucial to handle 3-CHLORO-5,6-DIPHENYL-1,2,4-TRIAZINE with caution due to its toxic nature and potential to cause irritation to the skin, eyes, and respiratory system upon exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 34177-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,1,7 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34177-11:
(7*3)+(6*4)+(5*1)+(4*7)+(3*7)+(2*1)+(1*1)=102
102 % 10 = 2
So 34177-11-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H10ClN3/c16-15-17-13(11-7-3-1-4-8-11)14(18-19-15)12-9-5-2-6-10-12/h1-10H

34177-11-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Chloro-5,6-diphenyl-1,2,4-triazine

1.2 Other means of identification

Product number -
Other names HMS1580H14

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:34177-11-2 SDS

34177-11-2Relevant academic research and scientific papers

Synthesis of Isoquinolines by Cycloaddition of Arynes to 1,2,4-Triazines

Gonsalves, Antonio M. d'A. Rocha,Melo, Teresa M. V. D. Pinho e

, p. 6821 - 6826 (2007/10/02)

Benzyne has been generated from benzenediazonium-2-carboxylate in the presence of several 1,2,4-triazines 1 and isoquinolines 2 have been isolated in moderate yield. 1-Aminobenzotriazole was also used as the source of benzyne and isoquinolines were again isolated in moderate yield from these reactions. 4-Methylbenzyne, which was generated from 5-methylanthranilic acid, reacted unselectively with the triazines to give mixtures of 6- and 7-methylisoquinolines 3 and 4.On the other hand reactions of 3-methylbenzyne with the triazines 1d and 1e proceeded with high regioselectivity, giving only the 5-methylisoquinoline 5a and the 8-methylisoquinoline 6b, respectively.

Metal-assisted Reactions: Part 19. Burst Kinetics in Heterogeneous Catalytic Transfer Hydrogenolysis

Johnstone, Robert A. W.,Price, Peter J.

, p. 1069 - 1076 (2007/10/02)

Arene formation by catalytic transfer hydrogenolysis of aryloxytetrazolyl ethers in the liquid-phase shows biphasic concentration-time curves which indicate rate-limiting dissociation of heterogeneous complexes between catalyst and one of the reaction products, a tetrazolone.A dependence of catalytic reaction rate on pH and following modifications made to the catalyst are reported also.

Pharmacologically active substituted 1,2,4-triazines

-

, (2008/06/13)

Substituted 1,2,4-triazines, compositions thereof and methods of using same are described. The compounds of the invention exhibit a wide range of pharmacological activity including anti-inflammatory, analgesic, anti-pyretic, hypotensive and central nervous system effects.

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