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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)-

(S);-1-(2,3-Difluorophenyl);ethanamine hydrochloride

C[C@@H](c1cccc(c1F)F)N.Cl Request for Quotation
Chemical Name: (S);-1-(2,3-Difluorophenyl);ethanamine hydrochloride
CAS Number: 1415303-43-3
Product Number: AG001GJT(AGN-PC-0WCZVA)
Synonyms:
MDL No:
Molecular Formula: C8H10ClF2N
Molecular Weight: 193.6215

Identification/Properties

Computed Properties
Molecular Weight:
193.622g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
193.047g/mol
Monoisotopic Mass:
193.047g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
129
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-1-(2,3-Difluorophenyl)ethanamine hydrochloride is a valuable compound utilized in chemical synthesis, particularly in the field of pharmaceutical research and development. This chiral amine derivative plays a crucial role as a building block in the creation of various biologically active molecules. Its unique chemical structure and stereochemistry make it a versatile intermediate for the synthesis of diverse pharmaceutical compounds, including potential drug candidates and new chemical entities. By incorporating (S)-1-(2,3-Difluorophenyl)ethanamine hydrochloride into synthetic pathways, chemists can access a wide range of structurally complex and pharmacologically relevant molecules with enhanced biological activities and improved therapeutic properties.