56617-00-6

Basic information

• Product Name: 3-bromo-1-phenyl-1H-1,2,4-triazole
• Synonyms: 3-bromo-1-phenyl-1H-1,2,4-triazole
• CAS NO: 56617-00-6
• Molecular Weight: 224.06
• Mol File: 56617-00-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-bromo-1-phenyl-1H-1,2,4-triazole(CAS DataBase Reference)
• NIST Chemistry Reference: 3-bromo-1-phenyl-1H-1,2,4-triazole(56617-00-6)
• EPA Substance Registry System: 3-bromo-1-phenyl-1H-1,2,4-triazole(56617-00-6)

Safety Data

• Hazardous Substances Data: 56617-00-6(Hazardous Substances Data)

Upstream product

• 7343-33-1 3-bromo-1H-1,2,4-triazole 
• 98-80-6 phenylboronic acid 
• 31709-15-6 N-(1-phenyl-1H-1,2,4-triazol-3-yl)benzamide 
• 64781-78-8 3-diazo-3H-[1,2,4]triazole 
• 98-08-8 α,α,α-trifluorotoluene 
• 108-86-1 bromobenzene 

Relevant articles and documents

MOLECULES HAVING CERTAIN PESTICIDAL UTILITIES, AND INTERMEDIATES, COMPOSITIONS, AND PROCESSES RELATED THERETO

This disclosure relates to compounds having pesticidal utility against pests in phyla Nematoda, Arthropoda, and/or Mollusca, processes to produce such compounds and intermediates used in such processes, compositions containing such compounds, and processes of using such compounds against such pests. These compounds/molecules may be used, for example, as nematicides, acaricides, insecticides, miticides, and/or molluscicides. This document discloses compounds having the following formula (Formula One and/or Formula One-A).

TRIAZOLES FOR THE TREATMENT OF DEMYELINATING DISEASES

The invention relates to triazole compounds of formula I and I' or pharmaceutically acceptable salts thereof, useful as modulators of demyelinating diseases: The invention also provides pharmaceutically acceptable compositions comprising the compounds of the invention, methods of using the compositions and kits thereof in the treatment of various demyelinating and neurodegenerative diseases, including multiple sclerosis.

SUBSTITUENT AND COORDINATION EFFECTS IN SINGLET REACTIONS OF 3-DIAZO-3H-1,2,4-TRIAZOLES WITH SUBSTITUTED BENZENES AND NITRO COMPOUNDS

3-Diazo-3H-1,2,4-triazoles convert to singlet 3H-1,2,4-triazol-3-ylidenes which (1) effect directed electrophilic substitutions of benzenes and (2) coordinate with benzenoid substituents and nitro compounds to give decomposition or rearrangement products.