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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)-

Benzenemethanamine, 3-fluoro-a-methyl-, hydrochloride, (aS)-

Fc1cccc(c1)[C@@H](N)C.Cl Request for Quotation
Chemical Name: Benzenemethanamine, 3-fluoro-a-methyl-, hydrochloride, (aS)-
CAS Number: 321429-48-5
Product Number: AG007HD9(AGN-PC-0R7FJH)
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:
1
Exact Mass:
175.056g/mol
Monoisotopic Mass:
175.056g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
105
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-1-(3-Fluorophenyl)ethylamine hydrochloride, also known as $name$, is a valuable compound in chemical synthesis due to its versatile applications. This compound serves as a key building block for the construction of various pharmaceuticals, agrochemicals, and other fine chemicals. Its chiral nature makes it particularly useful in asymmetric synthesis, where the stereochemistry of the molecule plays a crucial role in determining its biological activity or other properties.In chemical synthesis, (S)-1-(3-Fluorophenyl)ethylamine hydrochloride can be used as a starting material for the preparation of chiral ligands, catalysts, and pharmacologically active molecules. Its incorporation into organic syntheses allows for the creation of enantiopure compounds, which are essential in drug discovery and development processes. Additionally, this compound can participate in various reactions such as reductive amination, cross-coupling reactions, and nucleophilic additions, enabling the efficient formation of complex molecular structures.Overall, (S)-1-(3-Fluorophenyl)ethylamine hydrochloride is an indispensable tool in the hands of synthetic chemists, enabling the creation of diverse compounds with tailored properties and functionalities.