57459-15-1

Basic information

• Product Name: 1,3,4-Oxathiazol-2-one, 5-[3-(trifluoromethyl)phenyl]-
• Synonyms: 5-(3-trifluoromethyl-phenyl)-[1,3,4]oxathiazol-2-one;5-(3-Trifluormethylphenyl)-1,3,4-oxathiazol-2-on;5-(α,α,α-trifluoro-m-tolyl)-1,3,4-oxathiazol-2-one;5-(3-(trifluoromethyl)phenyl)-1,3,4-oxathiazol-2-one;5-<3-(trifluoromethyl)-phenyl>-1,3,4-oxathiazol-2-one
• CAS NO: 57459-15-1
• Molecular Formula: C9H4F3NO2S
• Molecular Weight: 247.197
• Mol File: 57459-15-1.mol
• Article Data: 4

Chemical Properties

• Melting Point: 85 - 86.5 °C
• CAS DataBase Reference: 1,3,4-Oxathiazol-2-one, 5-[3-(trifluoromethyl)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,4-Oxathiazol-2-one, 5-[3-(trifluoromethyl)phenyl]-(57459-15-1)
• EPA Substance Registry System: 1,3,4-Oxathiazol-2-one, 5-[3-(trifluoromethyl)phenyl]-(57459-15-1)

Safety Data

• Hazardous Substances Data: 57459-15-1(Hazardous Substances Data)

Usage

Chemical family

Oxathiazolone

Type of compound

Heterocyclic

Ring structure

Contains oxygen, sulfur, and nitrogen atoms

Trifluoromethyl group

Attached to a phenyl ring

Chemical properties

Unique due to the trifluoromethyl group

Potential applications

Pharmaceutical and agrochemical industries

Biological activities

Antimicrobial, antifungal, and antioxidant properties

Research implications

Development of new drugs and agrochemicals with improved efficacy and safety profiles
This list provides a concise overview of the key characteristics and potential uses of 1,3,4-Oxathiazol-2-one, 5-[3-(trifluoromethyl)phenyl]-.

Upstream product

• 1801-10-1 3-trifluoromethylbenzamide 
• 2757-23-5 chloro(chlorosulfanyl)methanone 

Downstream Products

• 57459-27-5 [3-(3-trifluoromethyl-phenyl)-[1,2,4]thiadiazol-5-yl]-acetonitrile 
• 67048-80-0 5-phenyl-3-(3-trifluoromethyl-phenyl)-isothiazole-4-carboxylic acid ethyl ester 
• 76010-57-6 methyl 2-<3<(3-trifluoromethyl)phenyl>-1,2,4-thiadiazol-5-yl>benzoate 
• 57459-25-3 {bis-[3-(3-trifluoromethyl-phenyl)-[1,2,4]thiadiazol-5-yl]-methylene}-malononitrile 
• 57459-17-3 [3-(3-trifluoromethyl-phenyl)-[1,2,4]thiadiazol-5-yl]-ethenetricarbonitrile 
• 340174-49-4 2,3-bis-[3-(3-trifluoromethyl-phenyl)-[1,2,4]thiadiazol-5-yl]-but-2-enedinitrile 
• 57459-30-0 bis-[3-(3-trifluoromethyl-phenyl)-[1,2,4]thiadiazol-5-yl]-methanone 
• 67048-99-1 3-(3-trifluoromethyl-phenyl)-isothiazole-4-carboxylic acid ethyl ester 
• 67048-95-7 3-(3-trifluoromethyl-phenyl)-isothiazole-5-carboxylic acid ethyl ester 
• 67048-78-6 5-phenyl-3-(3-trifluoromethyl-phenyl)-isothiazole-4-carboxylic acid 
• 50483-80-2 3-(3-trifluoromethyl-phenyl)-[1,2,4]thiadiazole-5-carboxylic acid ethyl ester 

Relevant articles and documents

Synthesis of spiroindene-1,3-dione isothiazolines via a cascade michael/1,3-dipolar cycloaddition reaction of 1,3,4-oxathiazol-2-one and 2-arylidene-1,3-indandiones

The reaction of 1,3,4-oxathiazol-2-one derivative with 2-arylidene-1,3-indandione to furnish novel spiroindene-1,3-dione isothiazoline derivatives by Michael/1,3-dipolar [3+2]-cycloaddition reaction was investigated. The key 1,3-dipolar cycloaddition reaction step was examined in toluene solvent at reflux temperature to obtain mixture of two regioisomers (6a and 6b – 14a and 14b) and single isomers (15–20). The scope of this new reaction was demonstrated with many examples with high reactivity and yields.

3-Aryl-4-isothiazolecarboxylic acid and 3-aryl-4-isoxazolecarboxylic acid derivatives and their use as herbicides

Carboxylic acid derivatives having the formula STR1 have been found to be effective herbicides. They are especially effective when applied as a pre-emergent herbicide.