2,2,2-trifluoro-1-(1,3-oxazol-2-yl)ethanone


Chemical Name: 2,2,2-trifluoro-1-(1,3-oxazol-2-yl)ethanone
CAS Number: 898758-70-8
Product Number: AG00IFV6(AGN-PC-07ATSI)
Synonyms:
MDL No: MFCD07699301
Molecular Formula: C5H2F3NO2
Molecular Weight: 165.0701

Identification/Properties


Computed Properties
Molecular Weight:
165.071g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
165.004g/mol
Monoisotopic Mass:
165.004g/mol
Topological Polar Surface Area:
43.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
168
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



2-(Trifluoroacetyl)oxazole is a versatile compound widely utilized in chemical synthesis as a key building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. This molecule plays a crucial role in the construction of diverse organic compounds due to its unique properties and reactivity. In particular, 2-(Trifluoroacetyl)oxazole serves as an important intermediate in the synthesis of heterocyclic compounds, which are essential in drug development and materials science. By acting as a precursor in various chemical reactions, this compound enables the efficient and cost-effective production of complex molecules with specific biological or physical properties. Its ability to undergo diverse transformations makes it a valuable tool for chemists in designing and synthesizing novel compounds for a wide range of applications.