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5-CHLORO-3,6-DIPHENYL-1,2,4-TRIAZINE is a chemical compound characterized by the molecular formula C15H10ClN3. It is a triazine derivative featuring a chlorine atom and two phenyl groups, known for its role as an intermediate in the synthesis of pharmaceuticals, dyes, agrochemicals, and polymers, as well as a starting material for other organic compounds. This white solid is typically managed under controlled conditions due to its potential health and environmental risks.

94398-27-3

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94398-27-3 Usage

Uses

Used in Pharmaceutical Industry:
5-CHLORO-3,6-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 Dye Industry:
In the dye industry, 5-CHLORO-3,6-DIPHENYL-1,2,4-TRIAZINE is utilized as a precursor in the production of dyes, enhancing color properties and performance in various applications.
Used in Agrochemical Industry:
5-CHLORO-3,6-DIPHENYL-1,2,4-TRIAZINE is employed as a starting material in the synthesis of agrochemicals, aiding in the development of effective pesticides and other agricultural products.
Used in Polymer Industry:
5-CHLORO-3,6-DIPHENYL-1,2,4-TRIAZINE is used as a component in the production of polymers, contributing to the creation of materials with specific properties for various industrial applications.
Used in Organic Chemistry:
5-CHLORO-3,6-DIPHENYL-1,2,4-TRIAZINE serves as a starting material for the preparation of other organic compounds, facilitating the advancement of organic chemistry and the synthesis of novel molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 94398-27-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,3,9 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 94398-27:
(7*9)+(6*4)+(5*3)+(4*9)+(3*8)+(2*2)+(1*7)=173
173 % 10 = 3
So 94398-27-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H10ClN3/c16-14-13(11-7-3-1-4-8-11)18-19-15(17-14)12-9-5-2-6-10-12/h1-10H

94398-27-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 5-chloro-3,6-diphenyl-[1,2,4]triazine

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:94398-27-3 SDS

94398-27-3Relevant academic research and scientific papers

The Chemistry of 1,2,4-Triazines, XIV. - Synthesis and Reactions of 5-Chloro-1,2,4-triazines

Neunhoeffer, Hans,Reichel, Diethard,Cullmann, Birgit,Rehn, Ingrid

, p. 631 - 640 (2007/10/02)

5-Chloro-1,2,4-triazines 4 are prepared from 1,2,4-triazin-5(2H)-ones 3 and transfered into 5-amino- (7), 5-cyano (8), and 5-(ω-alkinyloxy)-1,2,4-triazines (9). 7a-d are cyclized to imidazo1,2,4-triazines (10a-d).

STUDIES ON as-TRIAZINE DERIVATIVES. VIII. SYNTHESIS OF 5-SUBSTITUTED 1,2,4-TRIAZINES

Konno, Shoetsu,Ohba, Setsuya,Agata, Mitsuko,Aizawa, Yuichi,Sagi, Mataichi,Yamanaka, Hiroshi

, p. 3259 - 3264 (2007/10/02)

Dehydroxy-chlorination of 6-methyl-3-phenyl (3a), and 3,6-diphenyl-5-oxo-2,5-dihydro-1,2,4-triazine (3b) afforded the corresponding 5-chloro-1,2,4-triazines (4a,b).The chloro-1,2,4-triazines (4a,b) treated with sodium alkoxides or amines to give the 5-alk

STUDIES ON as-TRIAZINE DERIVATIVES. IV. SYNTHESIS OF UNSYMMETRICAL 5,6-DISUBSTITUTED 1,2,4-TRIAZINES

Konno, Shoetsu,Sagi, Mataichi,Agata, Mitsuko,Aizawa, Yuichi,Yamanaka, Hiroshi

, p. 2241 - 2244 (2007/10/02)

The reaction of 5-chloro-6-methyl-3-phenyl-1,2,4-triazine (4a) with ethylidenetriphenylphosphorane followed by the hydrolysis of the resulting as-triazinylphosphorane afforded 5-ethyl-6-methyl-3-phenyl-1,2,4-triazine (6a) in 88 percent yield.The condensat

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