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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)-

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

COc1ccccc1C(C(F)(F)F)N.Cl Request for Quotation
Chemical Name: 2,2,2-Trifluoro-1-(2-methoxyphenyl)ethanamine hydrochloride
CAS Number: 1228880-25-8
Product Number: AG000JP1(AGN-PC-0WAM93)
Synonyms:
MDL No: MFCD11841105
Molecular Formula: C9H11ClF3NO
Molecular Weight: 241.6379

Identification/Properties

Computed Properties
Molecular Weight:
241.638g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
241.048g/mol
Monoisotopic Mass:
241.048g/mol
Topological Polar Surface Area:
35.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
183
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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 compound 2,2,2-Trifluoro-1-(2-methoxyphenyl)ethanamine hydrochloride plays a crucial role in chemical synthesis as a versatile intermediate. Its unique chemical structure enables it to participate in a variety of reactions, making it valuable for the creation of various organic compounds. This compound is particularly useful in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals due to its ability to introduce specific functional groups with precision. Additionally, its trifluoromethyl group imparts desirable properties to the final products, such as increased metabolic stability and improved pharmacokinetic profiles. By incorporating 2,2,2-Trifluoro-1-(2-methoxyphenyl)ethanamine hydrochloride into synthetic pathways, chemists can efficiently access a wide range of organic molecules with enhanced bioactivity and tailored physical characteristics.