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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-fluoro-2-nitrophenyl)-

CC(=O)Nc1ccc(cc1[N+](=O)[O-])F Request for Quotation
Chemical Name: Acetamide, N-(4-fluoro-2-nitrophenyl)-
CAS Number: 448-39-5
Product Number: AG003LDG(AGN-PC-0JMORR)
Synonyms:
MDL No:
Molecular Formula: C8H7FN2O3
Molecular Weight: 198.1512

Identification/Properties

Properties
MP:
71-73 °C(lit.);
BP:
383°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
198.153g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
198.044g/mol
Monoisotopic Mass:
198.044g/mol
Topological Polar Surface Area:
74.9A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
241
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#:
N/A
Hazard Statements:
H315-H319
Precautionary Statements:
P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(4-Fluoro-2-nitrophenyl)acetamide is a versatile compound widely used in organic chemical synthesis. This compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and advanced materials. Its unique structure and reactivity make it a crucial intermediate in the synthesis of complex organic molecules.In chemical synthesis, N-(4-Fluoro-2-nitrophenyl)acetamide can participate in a range of reactions including nucleophilic substitution, acylation, and reductive transformations. It can be utilized to introduce the 4-fluoro-2-nitrophenyl and acetamide functional groups into target molecules, thereby modulating their properties and biological activities.Furthermore, the presence of the nitro and fluoro substituents in this compound offers opportunities for further derivatization through reduction, functional group interconversion, or transition metal-catalyzed reactions. This enables chemists to access diverse chemical space and tailor the compound for specific applications in medicinal chemistry, materials science, and other interdisciplinary fields.Overall, the strategic use of N-(4-Fluoro-2-nitrophenyl)acetamide in chemical synthesis empowers researchers to access novel molecular architectures and develop innovative compounds with potential applications in various industrial sectors.