8-Bromo-6-trifluoromethyl[1,2,4]triazolo[1,5-a]pyridine - Names and Identifiers
Name | 8-Bromo-6-trifluoromethyl[1,2,4]triazolo[1,5-a]pyridine
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Synonyms | 8-Bromo-6-trifluoromethyl[1,2,4]triazolo[1,5-a]pyridine 8-BroMo-6-trifluoroMethyl[1,2,4]-Triazolo[1,5-a]pyridine [1,2,4]Triazolo[1,5-a]pyridine, 8-bromo-6-(trifluoromethyl)- 8-BROMO-6-TRIFLUOROMETHYL[1,2,4]TRIAZOLO[1,5-A]PYRIDINE(WXFC0359)
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CAS | 1170302-00-7
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8-Bromo-6-trifluoromethyl[1,2,4]triazolo[1,5-a]pyridine - Physico-chemical Properties
Molecular Formula | C7H3BrF3N3
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Molar Mass | 266.02 |
Storage Condition | Room Temprature |
Sensitive | IRRITANT |
MDL | MFCD12026327 |
8-Bromo-6-trifluoromethyl[1,2,4]triazolo[1,5-a]pyridine - Introduction
8-Bromo-6-trifluoromethyl[1,2,4]triazolo[1,5-a]pyridine is an organic compound with the chemical formula C7H3BrF3N4. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
-Appearance: Colorless or yellow solid
-melting point: about 180-182 ℃
-Solubility: Easily soluble in organic solvents such as dichloromethane and ethanol, slightly soluble in water
-Chemical properties: It is a heterocyclic compound containing bromine and trifluoromethyl groups, with the electronegativity of fluorine atoms and the electrophilicity of bromine atoms. Can participate in a series of organic reactions.
Use:
-Chemical synthesis: It can be used as a reagent and intermediate in organic synthesis. In organic synthesis reactions, it can be used to construct the skeleton of a variety of organic compounds, such as heterocycles, fluorine-containing compounds, etc.
-Pesticides and medicines: The structure of this compound makes it potentially pesticide and pharmaceutical activity. It can be used as a starting point for pesticide and pharmaceutical research for the synthesis of new pesticide and pharmaceutical molecules.
Preparation Method:
-This compound can be synthesized by a variety of methods, and the specific synthesis route depends on the required structure and reaction conditions. A common preparation method involves the addition of bromine and trifluoromethyl groups in a series of steps starting from p-aminobenzoic acid.
Safety Information:
-Follow the safe practices of the chemical laboratory and wear personal protective equipment such as lab coats, glasses and gloves.
-The compound has a certain toxicity and should be placed in a sealed container and kept away from fire and high temperature.
-During use, the risk of skin contact, inhalation and ingestion should be strictly controlled, and contact with eyes and mucous membranes should be avoided.
-When handling and disposing of waste, it should be handled and disposed in accordance with local environmental regulations to avoid harm to the environment.
Last Update:2024-04-09 02:00:56