1. Home
  2. (R)-1-(4-((Trifluoromethyl)thio)phenyl)ethanamine hydrochloride

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

(R)-1-(4-((Trifluoromethyl)thio)phenyl)ethanamine hydrochloride

C[C@H](c1ccc(cc1)SC(F)(F)F)N.Cl Request for Quotation
Chemical Name: (R)-1-(4-((Trifluoromethyl)thio)phenyl)ethanamine hydrochloride
CAS Number: 1800240-39-4
Product Number: AG0021M5(AGN-PC-0WAMAL)
Synonyms:
MDL No:
Molecular Formula: C9H11ClF3NS
Molecular Weight: 257.7035

Identification/Properties

Computed Properties
Molecular Weight:
257.699g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
257.025g/mol
Monoisotopic Mass:
257.025g/mol
Topological Polar Surface Area:
51.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
175
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The application of (R)-1-(4-((Trifluoromethyl)thio)phenyl)ethanamine hydrochloride in chemical synthesis lies in its utility as a versatile building block for the creation of various compounds. With its unique molecular structure, this compound serves as a valuable precursor in the synthesis of pharmaceuticals, agrochemicals, and materials science. Its incorporation in chemical reactions allows for the introduction of the trifluoromethylthio group, providing a powerful tool for modifying the physicochemical properties of target molecules. Additionally, the chiral nature of this compound, exhibiting an R-configuration, offers opportunities for enantioselective synthesis, enabling the production of optically pure compounds with enhanced biological activities. In summary, (R)-1-(4-((Trifluoromethyl)thio)phenyl)ethanamine hydrochloride serves as a strategic building block in chemical synthesis, contributing to the development of various functional materials and bioactive compounds.