Product Description
Chemical Name: 2-Amino-4-trifluoromethyloxazole
Synonyms : 2-Amino-4-trifluoromethyloxazole|
4-(trifluoromethyl)-1,3-oxazol-2-amine|
2-amino-4-(trifluoromethyl)oxazole|
4-Trifluoromethyl-oxazol-2-ylamine|
2-Oxazolamine,4-(trifluoromethyl)-
CAS No : 35629-71-1
Purity : 98%
Molecular Formula :C4H3F3N2O
Molecular Weight: 152.1
Appearance: Solid
High Stability and Purity for Reliable ResearchWith a melting point of 8487C and chemical stability under proper storage conditions, 2-Amino-4-trifluoromethyloxazole provides researchers with a reliable reagent or intermediate. Its >98% purity ensures consistent results in demanding analytical or synthetic applications, making it a trusted choice for discovery and development in pharmaceutical and agrochemical fields.
Convenient Packaging and Safe HandlingAvailable in sealed bottles of 1g, 5g, or 10g, this compound is easy to store and transport. While not classified as highly toxic and viewed as non-hazardous for shipping, users should still avoid contact with eyes, skin, or inhalation due to possible irritation, and follow chemical safety protocols during handling.
Diverse Applications in Chemical ResearchAs an intermediate, 2-Amino-4-trifluoromethyloxazole is instrumental in organic synthesis, particularly for pharmaceutical and crop-protection agents. The inclusion of a trifluoromethyl group increases its reactivity and utility, supporting innovative projects in academic, industrial, and contract research settings.
FAQs of 2-Amino-4- trifluoromethyloxazole:
Q: How should 2-Amino-4-trifluoromethyloxazole be safely stored and handled?
A: It should be kept in an airtight container, in a cool, dry place, and protected from light. Although it is not highly toxic or hazardous for transport, avoid contact with skin, eyes, and inhalation, using standard safety equipment and protocols.
Q: What are the main uses of 2-Amino-4-trifluoromethyloxazole in research and industry?
A: This compound is primarily used as an intermediate for pharmaceutical and agrochemical synthesis, and as a reagent in a variety of chemical research and organic synthesis applications.
Q: When should this chemical be chosen over other intermediates?
A: Choose 2-Amino-4-trifluoromethyloxazole when electron-withdrawing trifluoromethyl functionality is required, or when high chemical stability and analytical purity are critical for your synthesis or research outcomes.
Q: Where is 2-Amino-4-trifluoromethyloxazole commonly utilized?
A: It is commonly utilized in research laboratories, chemical manufacturing firms, and industries focusing on pharmaceuticals and agrochemicalsprimarily for discovery and intermediate production stages.
Q: What is the process or route of synthesis for this compound?
A: 2-Amino-4-trifluoromethyloxazole is synthesized by cyclization from trifluoroacetylglycine, forming the oxazole ring with an added trifluoromethyl group.
Q: What are the benefits of using this compound in organic synthesis?
A: Benefits include its high chemical stability, electron-withdrawing trifluoromethyl group for enhanced reactivity, and its high purity, all contributing to more predictable and reproducible results in chemical research processes.