873-41-6

Basic information

• Product Name: 3,5,6-TRICHLORO-[1,2,4]TRIAZINE
• Synonyms: 3,5,6-TRICHLORO-[1,2,4]TRIAZINE;Trichloro-1,2,4-triazine
• CAS NO: 873-41-6
• Molecular Formula: C₃Cl₃N₃
• Molecular Weight: 184.4112
• Product Categories: Heterocycle-other series
• Mol File: 873-41-6.mol
• Article Data: 5

Chemical Properties

• Melting Point: 57-58℃
• Boiling Point: 337.3ºC at 760 mmHg
• Flash Point: 188.209ºC
• Appearance: /
• Density: 1.757g/cm3
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.586
• Storage Temp.: Inert atmosphere,Store in freezer, under -20°C
• PKA: -2.55±0.63(Predicted)
• CAS DataBase Reference: 3,5,6-TRICHLORO-[1,2,4]TRIAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5,6-TRICHLORO-[1,2,4]TRIAZINE(873-41-6)
• EPA Substance Registry System: 3,5,6-TRICHLORO-[1,2,4]TRIAZINE(873-41-6)

Safety Data

• Hazardous Substances Data: 873-41-6(Hazardous Substances Data)

Usage

Uses

3,5,6-Trichloro-[1,2,4]triazine (cas# 873-41-6) is a compound useful in organic synthesis.

InChI:InChI=1/C3Cl3N3/c4-1-2(5)8-9-3(6)7-1

Upstream product

• 4956-05-2 6-bromo-1,2,4-triazine-3,5(2H,4H)-dione 

Downstream Products

• 946403-38-9 5-N-benzylamino-3,6-dichloro-1,2,4-triazine 
• 946403-39-0 3,5-N,N-dibenzylamino-6-chloro-1,2,4-triazine 
• 114722-54-2 1,3-dichloro-6,7,8,9-tetrahydro-5H-cycloheptapyridine 
• 41789-37-1 2,6-dichloro-5-pyridylmethyl chloride 
• 83403-50-3 3,6-dichloro-N-phenyl-1,2,4-triazin-5-amine 
• 132434-83-4 5-phenyl-3,6-dichloro-1,2,4-triazine 
• 132434-85-6 5-phenylthio-3,6-dichloro-1,2,4-triazine 
• 132434-84-5 5-phenoxy-3,6-dichloro-1,2,4-triazine 
• 823-62-1 3,6-dichloro-1,2,4-triazine-5-amine 

Relevant articles and documents

Discovery of 1,2,4-triazine-based derivatives as novel neddylation inhibitors and anticancer activity studies against gastric cancer MGC-803 cells

Neddylation modification is often over-expressed in a variety of human tumor cells. Therefore, targeting neddylation pathway may represent a potential approach to the treatment of human tumors. Herein, we describe the discovery of a hit scaffold from our

HIV INHIBITING 1,2,4-TRIAZIN-6-ONE DERIVATIVES

The present invention relates to HIV replication inhibitors of formula (I) a N-oxide, a pharmaceutically acceptable addition salt, a quaternary amine or a stereochemically isomeric form thereof, wherein ring A and ring B represent phenyl, pyridyl, pyridaz

Heterocyclic Polyfluoro-compounds. Part 39. Preparation and some Nucleophilic Substitution Reactions of Trifluoro-1,2,4-triazine

Fluorination of trichloro-1,2,4-triazine over potassium fluoride at 450 deg C in a flow system yields trifluoro-(91percent) and 6-chloro-3,5-difluoro-1,2,4-triazine (5percent).The trifluorotriazine yields a dimer with time, which reverts to the monomer wi