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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-(p-tolyl)ethanamine hydrochloride

NC(C(F)(F)F)c1ccc(cc1)C.Cl Request for Quotation
Chemical Name: 2,2,2-Trifluoro-1-(p-tolyl)ethanamine hydrochloride
CAS Number: 1186195-01-6
Product Number: AG008104(AGN-PC-0WAMNO)
Synonyms:
MDL No: MFCD11226565
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:
159
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-(p-tolyl)ethanamine hydrochloride, also known as $name$, is a valuable chemical compound widely used in chemical synthesis processes. With its unique structure and properties, this compound serves as a versatile building block in the creation of various organic molecules. In particular, $name$ is commonly employed as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its trifluoromethyl group imparts desirable characteristics to the final products, such as improved metabolic stability and enhanced bioactivity. By incorporating $name$ into synthetic pathways, chemists can efficiently access diverse molecular structures with tailored properties, making it an indispensable tool in modern organic chemistry.