500889-65-6

Basic information

• Product Name: 1,2,4-BENZOTRIAZIN-3-AMINE, 7-BROMO-
• Synonyms: 1,2,4-BENZOTRIAZIN-3-AMINE, 7-BROMO-;3-AMINO-7-BROMO-1,2,4-BENZOTRIAZINE
• CAS NO: 500889-65-6
• Molecular Formula: C₇H₅BrN₄
• Molecular Weight: 225.05
• Mol File: 500889-65-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 428.3 °C at 760 mmHg
• Flash Point: 212.8 °C
• Appearance: /
• Density: 1.849 g/cm³
• Vapor Pressure: 1.53E-07mmHg at 25°C
• Refractive Index: 1.764
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1,2,4-BENZOTRIAZIN-3-AMINE, 7-BROMO-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,4-BENZOTRIAZIN-3-AMINE, 7-BROMO-(500889-65-6)
• EPA Substance Registry System: 1,2,4-BENZOTRIAZIN-3-AMINE, 7-BROMO-(500889-65-6)

Safety Data

• Hazardous Substances Data: 500889-65-6(Hazardous Substances Data)

Usage

General Description

1,2,4-Benzotriazin-3-amine, 7-bromo- is a chemical compound with the molecular formula C7H5BrN4. It is a derivative of benzotriazine and is commonly used in the field of organic chemistry for the synthesis of various pharmaceuticals and agrochemicals. The 7-bromo substitution on the benzotriazine ring imparts unique properties to the compound, making it useful in a variety of research and industrial applications. It is also known for its potential as a building block for the development of new compounds with specific biological activities. Overall, 1,2,4-Benzotriazin-3-amine, 7-bromo- is a versatile and important chemical with potential applications in drug discovery and development.

InChI:InChI=1/C7H5BrN4/c8-4-1-2-5-6(3-4)11-12-7(9)10-5/h1-3H,(H2,9,10,12)

Upstream product

• 5228-61-5 5-bromo-2-nitroaniline 

Downstream Products

• 929194-33-2 7-(2,6-dichloro-phenyl)-benzo[1,2,4]triazin-3-ylamine 
• 677297-90-4 7-(2,6-Dimethyl-phenyl)-benzo[1,2,4]triazin-3-ylamine 

Relevant articles and documents

Organic compound and organic electroluminescent device containing same

The invention relates to an organic compound, which is characterized by having a structure as shown in (1), wherein L1 and L2 are respectively and independently selected from a single bond, a substituted or unsubstituted C6-C30 arylene group or a substituted or unsubstituted C3-C30 heteroarylene group; Arl and Ar2 are respectively and independently selected from a substituted or unsubstituted C6-C30 aryl group or a substituted or unsubstituted C3-C30 heteroaryl group; R is halogen, a cyano group, an alkyl group, a substituted or unsubstituted C6-C30 aryl group or a substituted or unsubstituted C3-C30 heteroaryl group; and n represents an integer of 0-3.