229623-52-3

Basic information

• Product Name: 7-TrifluoroMethyl-benzo[d]isoxazol-3-ylaMine
• Synonyms: 7-TrifluoroMethyl-benzo[d]isoxazol-3-ylaMine;7-(TrifluoroMethyl)benzo[d]isoxazol-3-aMine
• CAS NO: 229623-52-3
• Molecular Formula: C8H5F3N2O
• Molecular Weight: 202.1333096
• Mol File: 229623-52-3.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 7-TrifluoroMethyl-benzo[d]isoxazol-3-ylaMine(CAS DataBase Reference)
• NIST Chemistry Reference: 7-TrifluoroMethyl-benzo[d]isoxazol-3-ylaMine(229623-52-3)
• EPA Substance Registry System: 7-TrifluoroMethyl-benzo[d]isoxazol-3-ylaMine(229623-52-3)

Safety Data

• Hazardous Substances Data: 229623-52-3(Hazardous Substances Data)

Usage

General Description

7-TrifluoroMethyl-benzo[d]isoxazol-3-ylaMine is a chemical compound that belongs to the class of benzoisoxazoles, which are heterocyclic compounds containing a benzene fused to an isoxazole ring. 7-TrifluoroMethyl-benzo[d]isoxazol-3-ylaMine is specifically substituted with a trifluoromethyl group at the 7 position of the benzene ring. It has potential applications in the field of pharmaceuticals and agrochemicals due to its unique structure and properties. It can be used as a building block in the synthesis of various bioactive molecules and as a potential drug candidate. However, the safety and potential hazards of this compound should be assessed before its practical applications.

Upstream product

• 146070-35-1 2-fluoro-3-(trifluoromethyl)benzonitrile 

Relevant articles and documents

Application of a recyclable fluorous oxime in the convenient synthesis of 3-amino-1,2-benzisoxazoles and 4-amino-1H-2,3-benzoxazines

A microwave-assisted, fluorous synthetic route to 3-amino-1,2- benzisoxazoles and 4-amino-1H-2,3-benzoxazines has been developed. The strategy comprises linking the respective 2-fluorobenzonitrile or 2-(bromomethyl) benzonitrile to a fluorous oxime tag to give an aryloxime intermediate which then undergoes cyclization with concomitant cleavage of the substrate-tag in acidic conditions to provide the desired product in good to moderate yields. In addition, the aryloxime intermediate could be subjected to further reactions to expand the compound library. The product could be easily separated using fluorous solid-phase extraction (F-SPE) and the fluorous ketone recovered could be converted back to the fluorous oxime and reused in the next run of the synthesis.

Isoxazolylbenzamides as insecticides

The present invention is directed to isoxazolyl and benzisoxazolyl benzamide compounds useful as insecticides.