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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-(4-chloro-3-fluorophenyl)ethanamine hydrochloride

C[C@@H](c1ccc(c(c1)F)Cl)N Request for Quotation
Chemical Name: (S)-1-(4-chloro-3-fluorophenyl)ethanamine hydrochloride
CAS Number: 1114559-11-3
Product Number: AG007AKC(AGN-PC-0NXNVB)
Synonyms:
MDL No:
Molecular Formula: C8H9ClFN
Molecular Weight: 173.6152

Identification/Properties

Computed Properties
Molecular Weight:
173.615g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
173.041g/mol
Monoisotopic Mass:
173.041g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
131
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:
1
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-(4-Chloro-3-fluorophenyl)ethanamine, also known as $name$, is a valuable compound widely used in chemical synthesis. This chiral amine plays a crucial role in asymmetric synthesis, serving as a key building block for the preparation of various pharmaceuticals, agrochemicals, and advanced materials.$name$ is commonly employed as a chiral intermediate in the pharmaceutical industry, where its enantiopure form is essential for the synthesis of biologically active compounds. By incorporating $name$ into the molecular structure of target molecules, chemists can access specific enantiomers with improved pharmacological properties and reduced side effects.In addition to its pharmaceutical applications, $name$ finds use in the synthesis of fine chemicals and specialty materials. The presence of a chiral center in $name$ enables precise control over the stereochemistry of the final product, making it highly valuable for the production of optically active compounds used in a range of industries.Overall, the versatile nature of (S)-1-(4-Chloro-3-fluorophenyl)ethanamine makes it a key player in synthetic chemistry, enabling chemists to access a wide array of chiral molecules with diverse applications.