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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)-2,2,2-Trifluoro-1-(2-methoxyphenyl)ethanamine hydrochloride

COc1ccccc1[C@@H](C(F)(F)F)N.Cl Request for Quotation
Chemical Name: (S)-2,2,2-Trifluoro-1-(2-methoxyphenyl)ethanamine hydrochloride
CAS Number: 1391397-32-2
Product Number: AG001ADW(AGN-PC-0WAGYX)
Synonyms:
MDL No:
Molecular Formula: C9H11ClF3NO
Molecular Weight: 241.6379496

Identification/Properties

Safety Information

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-2,2,2-Trifluoro-1-(2-methoxyphenyl)ethanamine hydrochloride is a versatile compound widely utilized in chemical synthesis. Its application in organic chemistry is paramount due to its unique chemical structure and properties. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Incorporating this compound in the synthesis of complex molecules allows for the introduction of fluorine and methoxy groups, leading to the development of new, potentially biologically active compounds. Its chiral nature also enables the production of enantiopure compounds, crucial in drug development and asymmetric synthesis. In summary, (S)-2,2,2-Trifluoro-1-(2-methoxyphenyl)ethanamine hydrochloride plays a pivotal role in advancing the field of chemical synthesis by facilitating the creation of diverse and structurally complex molecules.