55915-30-5

Basic information

• Product Name: 1H-1,2,4-Triazolium, 1,4-diphenyl-3-(phenylamino)-, bromide
• Synonyms: 1H-1,2,4-Triazolium, 1,4-diphenyl-3-(phenylamino)-, bromide;1H-1,2,4-Triazolium,1,4-diphenyl-3-(phenylamino)-,bromide;2,3,5,6-Tetraazabicyclo[2.1.1]hex-1-ene, 3,5,6-triphenyl-, monohydrobromide;2,4-triazolium, 1,4-diphenyl-3-(phenylamino)-1h- bromide;2,4-triazolium, 1,4-diphenyl-3-(phenylamino)-1h-bromide
• CAS NO: 55915-30-5
• Molecular Formula: C20H17N4·Br
• Molecular Weight: 393.29
• Mol File: 55915-30-5.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 447.6°Cat760mmHg
• Flash Point: 224.5°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 3.31E-08mmHg at 25°C
• CAS DataBase Reference: 1H-1,2,4-Triazolium, 1,4-diphenyl-3-(phenylamino)-, bromide(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-1,2,4-Triazolium, 1,4-diphenyl-3-(phenylamino)-, bromide(55915-30-5)
• EPA Substance Registry System: 1H-1,2,4-Triazolium, 1,4-diphenyl-3-(phenylamino)-, bromide(55915-30-5)

Safety Data

• Hazardous Substances Data: 55915-30-5(Hazardous Substances Data)

Usage

Explanation

Different sources of media describe the Explanation of 55915-30-5 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. The compound consists of a 1H-1,2,4-triazolium ring, which is a five-membered ring with three nitrogen atoms and two hydrogen atoms, and a phenylamino group, which is a phenyl group (a six-carbon ring with a hydrogen atom) attached to an amino group (a nitrogen atom with two hydrogen atoms).
3. Bromide salt derivative
3. The compound is used as a building block for the preparation of various heterocyclic compounds and pharmaceuticals, which are important in the development of new drugs and materials.
4. The compound has been studied for its potential to exhibit antimicrobial (fighting against microorganisms), anticancer (inhibiting the growth of cancer cells), and antiviral (inhibiting the replication of viruses) properties.
5. The bromide salt form of the compound allows for easier handling and storage compared to the free base form, making it more convenient for researchers and chemists to work with in the laboratory.

Structure

1H-1,2,4-Triazolium ring and a phenylamino group

Application

Organic synthesis and medicinal chemistry

Biological activities

Antimicrobial, anticancer, and antiviral properties

Easier handling and storage

Bromide salt form

InChI:InChI=1/C20H18N4.BrH/c1-4-10-17(11-5-1)21-20-22-24(19-14-8-3-9-15-19)16-23(20)18-12-6-2-7-13-18;/h1-15H,16H2,(H,21,22);1H