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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Acetamide, 2,2,2-trifluoro-N-(3-formylphenyl)-

O=Cc1cccc(c1)NC(=O)C(F)(F)F Request for Quotation
Chemical Name: Acetamide, 2,2,2-trifluoro-N-(3-formylphenyl)-
CAS Number: 152528-11-5
Product Number: AG019OTR(AGN-PC-0LWTMJ)
Synonyms:
MDL No:
Molecular Formula: C9H6F3NO2
Molecular Weight: 217.1446

Identification/Properties

Computed Properties
Molecular Weight:
217.147g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
217.035g/mol
Monoisotopic Mass:
217.035g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
252
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 2,2,2-Trifluoro-N-(3-formylphenyl)acetamide is a versatile chemical compound widely utilized in chemical synthesis for its unique properties and diverse reactivity. This compound serves as a valuable building block in the creation of various organic molecules due to its trifluoromethyl and formyl functional groups, which offer opportunities for selective transformations and derivatizations.In organic synthesis, 2,2,2-Trifluoro-N-(3-formylphenyl)acetamide can be employed as a key intermediate for the introduction of trifluoromethyl and formyl moieties into complex molecular structures. Its trifluoroacetyl group can participate in a range of synthetic reactions, including cross-coupling reactions, nucleophilic additions, and nucleophilic substitutions, enabling the synthesis of fluorinated compounds with enhanced properties.Furthermore, the formyl group in 2,2,2-Trifluoro-N-(3-formylphenyl)acetamide offers a reactive handle for subsequent functionalization, allowing for the construction of diverse chemical scaffolds and the preparation of advanced intermediates in medicinal chemistry, materials science, and agrochemical research.Overall, the strategic incorporation of 2,2,2-Trifluoro-N-(3-formylphenyl)acetamide in chemical synthesis facilitates the efficient and controlled manipulation of molecular frameworks, leading to the development of novel compounds with valuable applications in various fields of chemistry.