1-(4-BROMO-2-FLUOROPHENYL)ETHANAMINE|1034266-14-2,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

1-(4-BROMO-2-FLUOROPHENYL)ETHANAMINE

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Chemical Name:	1-(4-BROMO-2-FLUOROPHENYL)ETHANAMINE
CAS Number:	1034266-14-2
Product Number:	AG00966J(AGN-PC-0WAKF5)
Synonyms:
MDL No:
Molecular Formula:	C8H9BrFN
Molecular Weight:	218.0662

Identification/Properties
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Identification/Properties

Computed Properties

Molecular Weight:

218.069g/mol

XLogP3:

Hydrogen Bond Donor Count:

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Rotatable Bond Count:

Exact Mass:

216.99g/mol

Monoisotopic Mass:

216.99g/mol

Topological Polar Surface Area:

26A^2

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Formal Charge:

Complexity:

131

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Compound Is Canonicalized:

Yes

Safety Information

GHS Pictogram:

N/A

Signal Word:

UN#:

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Precautionary Statements:

Class:

Packing Group:

NMR Spectrum

Other Analytical Data

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Chemical Structure

1-(4-Bromo-2-fluorophenyl)ethanamine is a versatile chemical compound widely used in chemical synthesis. It serves as a key building block in the production of various pharmaceuticals, agrochemicals, and materials. With its unique combination of bromine and fluorine substituents, this compound offers valuable reactivity and selectivity in a range of synthetic transformations.In organic synthesis, 1-(4-Bromo-2-fluorophenyl)ethanamine plays a crucial role as a precursor in the preparation of biologically active molecules such as pharmaceutical intermediates and drug candidates. Its structure provides opportunities for further functionalization through a variety of reactions, including nucleophilic substitutions, palladium-catalyzed cross-coupling reactions, and transition metal-catalyzed transformations.Furthermore, this compound can be utilized in the synthesis of specialty chemicals and advanced materials due to its ability to introduce specific functional groups with precise spatial arrangements. By incorporating 1-(4-Bromo-2-fluorophenyl)ethanamine into synthetic routes, chemists can access diverse molecular architectures and tailor properties to meet desired specifications in fields ranging from medicine to materials science.Overall, the application of 1-(4-Bromo-2-fluorophenyl)ethanamine in chemical synthesis underscores its significance as a valuable intermediate with broad utility and potential for innovation in the development of novel compounds for various industrial applications.