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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, N-[4-(trifluoromethyl)phenyl]-

CC(=O)Nc1ccc(cc1)C(F)(F)F Request for Quotation
Chemical Name: Acetamide, N-[4-(trifluoromethyl)phenyl]-
CAS Number: 349-97-3
Product Number: AG003KBG(AGN-PC-0JIG08)
Synonyms:
MDL No:
Molecular Formula: C9H8F3NO
Molecular Weight: 203.1611

Identification/Properties

Properties
MP:
152-153°C
BP:
299℃
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
203.164g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
203.056g/mol
Monoisotopic Mass:
203.056g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
207
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P233-P260-P261-P264-P270-P271-P280-P301+P312-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P330-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(4-(Trifluoromethyl)phenyl)acetamide is a versatile compound commonly employed in chemical synthesis as a valuable building block. This compound is known for its unique reactivity and selectivity in various reactions, making it a popular choice in the development of new molecules and materials.In organic synthesis, N-(4-(Trifluoromethyl)phenyl)acetamide serves as a crucial intermediate for the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its trifluoromethyl group plays a key role in introducing fluorine atoms into organic molecules, which can enhance their biological activities or alter their physicochemical properties. Additionally, the phenylacetamide moiety provides a stable and versatile scaffold for further functionalization.Furthermore, N-(4-(Trifluoromethyl)phenyl)acetamide is often used in transition-metal-catalyzed cross-coupling reactions, such as Suzuki-Miyaura coupling and Heck reaction, to construct complex organic compounds. Its ability to undergo various transformations under mild conditions makes it a valuable tool for synthetic chemists aiming to streamline their processes and improve yields.Overall, N-(4-(Trifluoromethyl)phenyl)acetamide serves as a valuable reagent in chemical synthesis, offering a wide range of possibilities for designing and synthesizing novel molecules with diverse applications.