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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)-

Benzeneethanamine, b-fluoro-, hydrochloride

NCC(c1ccccc1)F.Cl Request for Quotation
Chemical Name: Benzeneethanamine, b-fluoro-, hydrochloride
CAS Number: 64068-24-2
Product Number: AG01AD35(AGN-PC-0TB5Z7)
Synonyms:
MDL No:
Molecular Formula: C8H11ClFN
Molecular Weight: 175.6310

Identification/Properties

Computed Properties
Molecular Weight:
175.631g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
175.056g/mol
Monoisotopic Mass:
175.056g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
89.3
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Fluoro-2-phenylethan-1-amine hydrochloride, also known as $name$, is a versatile chemical compound commonly used in chemical synthesis processes. This compound plays a crucial role as a key building block in the development of various pharmaceuticals, agrochemicals, and other fine chemicals. Due to its unique chemical structure, $name$ serves as an important intermediate in the synthesis of complex organic molecules.One of the primary applications of 2-Fluoro-2-phenylethan-1-amine hydrochloride in chemical synthesis is its use in medicinal chemistry to create novel drug candidates. By incorporating this compound into molecular structures, researchers can modify the pharmacological properties of potential drugs, enhancing their efficacy and reducing potential side effects. Additionally, $name$ is utilized in the synthesis of specialized reagents and catalysts, enabling the creation of new chemical transformations and processes.Moreover, 2-Fluoro-2-phenylethan-1-amine hydrochloride is employed in the development of agrochemicals to enhance crop protection and improve agricultural sustainability. By leveraging the unique reactivity and functional groups of this compound, chemists can design innovative pesticides and herbicides that target specific pests and pathogens effectively.Overall, the application of 2-Fluoro-2-phenylethan-1-amine hydrochloride in chemical synthesis encompasses a wide range of industries, from pharmaceuticals to agriculture, driving innovation and advancement in molecular design and synthetic chemistry.