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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-nitro-3-(trifluoromethyl)phenyl]-

CC(=O)Nc1ccc(c(c1)C(F)(F)F)[N+](=O)[O-] Request for Quotation
Chemical Name: Acetamide, N-[4-nitro-3-(trifluoromethyl)phenyl]-
CAS Number: 393-12-4
Product Number: AG003LUQ(AGN-PC-0JOJII)
Synonyms:
MDL No:
Molecular Formula: C9H7F3N2O3
Molecular Weight: 248.1587

Identification/Properties

Properties
MP:
108 °C
BP:
389.8°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
248.161g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
248.041g/mol
Monoisotopic Mass:
248.041g/mol
Topological Polar Surface Area:
74.9A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
314
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:
Danger
UN#:
3261
Hazard Statements:
H314
Precautionary Statements:
P260-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(4-Nitro-3-(trifluoromethyl)phenyl)acetamide, commonly known as $name$, is a versatile compound widely used in chemical synthesis processes. Its unique chemical structure allows it to serve as a key building block in the creation of various complex molecules and pharmaceutical intermediates.$name$ is particularly valued for its role as a precursor in the synthesis of novel pharmaceutical compounds. Its functional groups facilitate reactions leading to the formation of diverse molecular structures with potential biological activities. The nitro group in $name$ serves as a versatile handle for further functionalization, enabling the introduction of different substituents to modulate the properties of the final products.In addition to pharmaceutical applications, $name$ finds use in the preparation of specialty chemicals and advanced materials. Its trifluoromethyl group imparts unique physicochemical properties to the compounds derived from $name$, making them valuable in industries such as organic electronics, agrochemicals, and materials science.Overall, the versatility and reactivity of N-(4-Nitro-3-(trifluoromethyl)phenyl)acetamide make it a valuable tool in chemical synthesis, allowing for the efficient construction of diverse chemical architectures with potential applications in pharmaceuticals, materials, and beyond.