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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,2-chloro-6-fluoro-a-methyl-, (aS)-

C[C@@H](c1c(F)cccc1Cl)N Request for Quotation
Chemical Name: Benzenemethanamine,2-chloro-6-fluoro-a-methyl-, (aS)-
CAS Number: 1000922-53-1
Product Number: AG0000VQ(AGN-PC-0OPE7I)
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (S)-1-(2-Chloro-6-fluorophenyl)ethanamine is a versatile chemical compound widely used in organic synthesis processes. Its unique stereochemistry and functional groups make it a valuable building block in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals.One key application of (S)-1-(2-Chloro-6-fluorophenyl)ethanamine is as a chiral auxiliary in asymmetric synthesis. By utilizing the chiral nature of this compound, chemists can efficiently control the stereochemistry of reactions, leading to the formation of highly enantioenriched products. This is particularly valuable in the pharmaceutical industry, where chirality plays a crucial role in drug efficacy and safety.Additionally, (S)-1-(2-Chloro-6-fluorophenyl)ethanamine can serve as a precursor for the synthesis of various biologically active compounds. Its functional groups allow for the introduction of different moieties through selective chemical reactions, enabling the creation of diverse chemical structures with tailored properties.Overall, the versatility and unique properties of (S)-1-(2-Chloro-6-fluorophenyl)ethanamine make it an indispensable tool in the toolbox of chemists involved in the development of novel compounds with applications in pharmaceuticals, agrochemicals, and materials science.