94398-27-3

Basic information

• Product Name: 5-CHLORO-3,6-DIPHENYL-1,2,4-TRIAZINE
• Synonyms: 5-CHLORO-3,6-DIPHENYL-1,2,4-TRIAZINE
• CAS NO: 94398-27-3
• Molecular Formula: C₁₅H₁₀ClN₃
• Molecular Weight: 267.71
• Mol File: 94398-27-3.mol
• Article Data: 3

Chemical Properties

• Melting Point: 132-134°
• Boiling Point: 460.7°C at 760 mmHg
• Flash Point: 264.9°C
• Appearance: /
• Density: 1.265g/cm³
• Vapor Pressure: 3.12E-08mmHg at 25°C
• Refractive Index: 1.622
• CAS DataBase Reference: 5-CHLORO-3,6-DIPHENYL-1,2,4-TRIAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-CHLORO-3,6-DIPHENYL-1,2,4-TRIAZINE(94398-27-3)
• EPA Substance Registry System: 5-CHLORO-3,6-DIPHENYL-1,2,4-TRIAZINE(94398-27-3)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 94398-27-3(Hazardous Substances Data)

Usage

General Description

5-CHLORO-3,6-DIPHENYL-1,2,4-TRIAZINE is a chemical compound with the molecular formula C15H10ClN3. It is a triazine derivative that contains a chlorine atom and two phenyl groups. 5-CHLORO-3,6-DIPHENYL-1,2,4-TRIAZINE is commonly used as an intermediate in the synthesis of various pharmaceuticals, dyes, and agrochemicals. It is also used in the production of polymers and as a starting material for the preparation of other organic compounds. 5-CHLORO-3,6-DIPHENYL-1,2,4-TRIAZINE is a white solid that is typically handled and stored under controlled conditions due to its potential health and environmental hazards.

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

Upstream product

• 36214-25-2 3,6-diphenyl-4H-[1,2,4]triazin-5-one 
• 28819-30-9 benzamidrazone 
• 25131-36-6 N'-(cyano-phenyl-methylene)-benzohydrazonoyl chloride 
• 106474-32-2 4-nitroso-3,5-diphenyl-1H-pyrazole 
• 41940-16-3 3,6-diphenyl-5-methyl-1,2,4-triazine 
• 611-73-4 Benzoylformic acid 
• 36214-25-2 5-oxo-3,6-diphenyl-2,5-dihydro-as-triazine 
• 37496-81-4 N'-(cyano-phenyl-methylene)-benzamidrazone 

Downstream Products

• 126542-66-3 3,6-Diphenyl-5-undec-10-ynyloxy-[1,2,4]triazine 
• 126542-63-0 5-Hex-5-ynyloxy-3,6-diphenyl-[1,2,4]triazine 
• 129190-60-9 5-(2-Iodo-phenoxy)-3,6-diphenyl-[1,2,4]triazine 
• 116178-05-3 3,6-diphenyl-1,2,4-triazine-5-carbonitrile 
• 54637-94-4 5-methoxy-3,6-diphenyl-1,2,4-triazine 
• 107126-35-2 5-benzoyl-3,6-diphenyl-as-triazine 
• 94398-29-5 C₁₈H₁₇N₃OS 
• 94398-41-1 5-phenacyl-3,6-diphenyl-1,2,4-triazine 
• 116178-03-1 Cyano-(3,6-diphenyl-[1,2,4]triazin-5-yl)-acetic acid ethyl ester 
• 33063-35-3 3,6-diphenyl-[1,2,4]triazine 
• 94398-12-6 5-iodo-3,6-diohenyl-as-triazine 
• 41940-16-3 3,6-diphenyl-5-methyl-1,2,4-triazine 
• 94398-22-8 5-ethyl-3,6-diphenyl-1,2,4-triazine 
• 94398-43-3 5-acetyl-3,6-diphenyl-as-triazine 

Relevant articles and documents

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

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. IV. SYNTHESIS OF UNSYMMETRICAL 5,6-DISUBSTITUTED 1,2,4-TRIAZINES

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