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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)-

3-Amino-4,6-difluoro(trifluoromethoxy)benzene

Fc1cc(F)c(cc1OC(F)(F)F)N Request for Quotation
Chemical Name: 3-Amino-4,6-difluoro(trifluoromethoxy)benzene
CAS Number: 123572-59-8
Product Number: AG000KTH(AGN-PC-001FC5)
Synonyms:
MDL No:
Molecular Formula: C7H4F5NO
Molecular Weight: 213.1048

Identification/Properties

Properties
BP:
198.5°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
213.107g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
1
Exact Mass:
213.021g/mol
Monoisotopic Mass:
213.021g/mol
Topological Polar Surface Area:
35.2A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
197
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-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


The compound 2,4-Difluoro-5-(trifluoromethoxy)benzenamine, also known as $name$, is a versatile building block in chemical synthesis. Its unique structure, featuring a fluorine substitution pattern and a trifluoromethoxy group, makes it a valuable intermediate in the production of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, $name$ can be used as a key starting material for the preparation of complex organic molecules with specific properties and functions. Its fluorinated moieties offer opportunities for enhancing pharmacokinetic properties, improving bioavailability, and modulating the reactivity and selectivity of target compounds. The trifluoromethoxy group, in particular, is a useful directing group for introducing further functionalization at specific positions within the molecule.Furthermore, the presence of both fluorine and trifluoromethoxy substituents in $name$ can facilitate interactions with biological targets, such as enzymes or receptors, leading to the development of novel bioactive molecules with potential therapeutic applications. Additionally, the electron-withdrawing nature of the fluorine atoms can influence the physicochemical properties of the final products, including solubility, stability, and binding affinity.Overall, the strategic incorporation of 2,4-Difluoro-5-(trifluoromethoxy)benzenamine into synthetic pathways enables chemists to access a diverse array of structurally complex and biologically relevant compounds, making it a valuable tool in drug discovery, materials science, and other areas of chemical research.