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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)-

Benzene, 1-chloro-2-fluoro-5-nitro-3-(trifluoromethyl)-

[O-][N+](=O)c1cc(Cl)c(c(c1)C(F)(F)F)F Request for Quotation
Chemical Name: Benzene, 1-chloro-2-fluoro-5-nitro-3-(trifluoromethyl)-
CAS Number: 914225-55-1
Product Number: AG00GRPE(AGN-PC-05IXH4)
Synonyms:
MDL No:
Molecular Formula: C7H2ClF4NO2
Molecular Weight: 243.5429

Identification/Properties

Computed Properties
Molecular Weight:
243.542g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
0
Exact Mass:
242.971g/mol
Monoisotopic Mass:
242.971g/mol
Topological Polar Surface Area:
45.8A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
254
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:
H302-H315-H320-H335
Precautionary Statements:
P264-P270-P301+P312-P330
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Chloro-2-fluoro-5-nitro-3-(trifluoromethyl)benzene is a versatile compound utilized in chemical synthesis for various applications. This compound serves as a valuable building block in the development of pharmaceuticals, agrochemicals, and materials science. Its unique structure and reactive properties make it a key intermediate in the synthesis of complex organic molecules. Additionally, its trifluoromethyl group enhances the compound's stability and increases its potential for use in challenging reactions. Overall, 1-Chloro-2-fluoro-5-nitro-3-(trifluoromethyl)benzene plays a crucial role in the advancement of modern synthetic chemistry.