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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-(3-fluorophenyl)ethanamine;hydrochloride

Fc1cccc(c1)C(C(F)(F)F)N.Cl Request for Quotation
Chemical Name: 2,2,2-trifluoro-1-(3-fluorophenyl)ethanamine;hydrochloride
CAS Number: 1185302-13-9
Product Number: AG0092YF(AGN-PC-07HBFR)
Synonyms:
MDL No: MFCD10565658
Molecular Formula: C8H8ClF4N
Molecular Weight: 229.6024

Identification/Properties

Computed Properties
Molecular Weight:
229.603g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
229.028g/mol
Monoisotopic Mass:
229.028g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
168
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,2,2-Trifluoro-1-(3-fluorophenyl)ethylamine Hydrochloride, also known as $name$, is a versatile compound that finds extensive application in chemical synthesis. This compound is widely used as a key building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals due to its unique chemical properties.In chemical synthesis, $name$ plays a crucial role as a fluorinated amine, which can serve as a valuable intermediate in the preparation of complex molecules. Its trifluoromethyl and fluorophenyl groups are particularly valuable for introducing fluorine atoms into organic molecules, resulting in compounds with enhanced biological activity, improved metabolic stability, and altered physicochemical properties.$name$ is commonly employed in the synthesis of fluorinated drug candidates, agrochemicals with improved efficacy, and materials with unique properties. Its ability to introduce fluorine atoms in specific positions of a molecule enables chemists to tailor the properties of the final product, leading to compounds with enhanced bioavailability, target specificity, and environmental compatibility.Overall, the application of 2,2,2-Trifluoro-1-(3-fluorophenyl)ethylamine Hydrochloride in chemical synthesis is essential for the development of novel compounds with diverse applications in the pharmaceutical, agricultural, and materials science industries.