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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-[3-(TRIFLUOROMETHYL)PHENYL]ETHYLAMINE-HCl

C[C@@H](c1cccc(c1)C(F)(F)F)N.Cl Request for Quotation
Chemical Name: (S)-1-[3-(TRIFLUOROMETHYL)PHENYL]ETHYLAMINE-HCl
CAS Number: 1213939-94-6
Product Number: AG007Q9O(AGN-PC-0WA2TE)
Synonyms:
MDL No:
Molecular Formula: C9H11ClF3N
Molecular Weight: 225.6385

Identification/Properties

Computed Properties
Molecular Weight:
225.639g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
225.053g/mol
Monoisotopic Mass:
225.053g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
167
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-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (S)-1-(3-(Trifluoromethyl)phenyl)ethanamine hydrochloride is a versatile compound widely utilized in chemical synthesis processes. This compound serves as a valuable building block for the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structural properties make it a key ingredient in the development of chiral molecules, enabling the synthesis of enantiopure compounds with high optical purity. The (S)-1-(3-(Trifluoromethyl)phenyl)ethanamine hydrochloride is particularly valuable in asymmetric synthesis, where the stereochemistry of the compound plays a crucial role in determining its biological activity and performance. Its application extends to the creation of complex organic molecules, making it an essential tool for synthetic chemists in the pharmaceutical and chemical industries.