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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)-

Benzamide, 4-fluoro-3-(trifluoromethyl)-

NC(=O)c1ccc(c(c1)C(F)(F)F)F Request for Quotation
Chemical Name: Benzamide, 4-fluoro-3-(trifluoromethyl)-
CAS Number: 67515-57-5
Product Number: AG003LDR(AGN-PC-0JMTSB)
Synonyms:
MDL No:
Molecular Formula: C8H5F4NO
Molecular Weight: 207.1250

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
207.128g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
207.031g/mol
Monoisotopic Mass:
207.031g/mol
Topological Polar Surface Area:
43.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
228
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-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Fluoro-3-(trifluoromethyl)benzamide, also known by its chemical formula C8H4F4NO, is a versatile compound widely utilized in chemical synthesis. This unique compound serves as a valuable building block in organic chemistry due to its distinctive structure and reactivity.In chemical synthesis, 4-Fluoro-3-(trifluoromethyl)benzamide is employed as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and advanced materials. Its trifluoromethyl group provides enhanced stability and lipophilicity to the final products, making it particularly advantageous for drug discovery and development.Furthermore, the fluoro substituent on the benzene ring offers opportunities for selective functionalization through various chemical reactions, such as nucleophilic aromatic substitution and transition metal-catalyzed cross-coupling reactions. This enables chemists to efficiently introduce diverse functional groups and structural motifs into organic molecules, expanding the scope of potential applications for this versatile compound.Overall, 4-Fluoro-3-(trifluoromethyl)benzamide plays a pivotal role in modern chemical synthesis by facilitating the construction of complex molecules with enhanced properties and functionalities, making it a valuable tool for researchers in the field of organic chemistry.