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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)-

1-[3,5-bis(trifluoromethyl)phenyl]ethanamine;hydrochloride

CC(c1cc(cc(c1)C(F)(F)F)C(F)(F)F)N.Cl Request for Quotation
Chemical Name: 1-[3,5-bis(trifluoromethyl)phenyl]ethanamine;hydrochloride
CAS Number: 374822-27-2
Product Number: AG003DTA(AGN-PC-03NH1J)
Synonyms:
MDL No: MFCD24335266
Molecular Formula: C10H10ClF6N
Molecular Weight: 293.6365

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid

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


1-[3,5-Bis(trifluoromethyl)phenyl]ethanamine Hydrochloride is a versatile compound commonly used in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block for the synthesis of various organic molecules, thanks to its functional group flexibility and stability under a wide range of reaction conditions. In particular, this compound is frequently employed in the formation of complex pharmaceutical intermediates, agrochemicals, and specialty materials. Its trifluoromethylphenyl moiety imparts enhanced chemical and physical properties to the resulting products, making it a valuable tool in the development of novel compounds with improved performance characteristics. Additionally, the ethanamine functionality provides a handle for further structural modifications, enabling chemists to fine-tune the properties of the target molecules.