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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)-

Benzenemethanamine, N-ethyl-4-(trifluoromethyl)-

CCNCc1ccc(cc1)C(F)(F)F Request for Quotation
Chemical Name: Benzenemethanamine, N-ethyl-4-(trifluoromethyl)-
CAS Number: 90390-12-8
Product Number: AG003SZU(AGN-PC-0JRTA5)
Synonyms:
MDL No: MFCD09948554
Molecular Formula: C10H12F3N
Molecular Weight: 203.2042

Identification/Properties

Properties
BP:
208.3°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
203.208g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
203.092g/mol
Monoisotopic Mass:
203.092g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
159
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
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


N-Ethyl-4-(trifluoromethyl)benzylamine is a versatile compound widely used in chemical synthesis as a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. It serves as a valuable building block due to its unique structural features and reactivity.This compound is often employed in the synthesis of complex organic molecules through various reactions such as nucleophilic substitution, reductive amination, and cross-coupling reactions. Its trifluoromethyl group enhances the lipophilicity and electronic properties of the molecules, making it particularly useful in medicinal chemistry for enhancing drug potency and selectivity.Additionally, N-Ethyl-4-(trifluoromethyl)benzylamine can act as a chiral auxiliary in asymmetric synthesis, enabling the stereoselective construction of enantioenriched compounds. Its presence can significantly influence the stereochemical outcome of reactions, making it a valuable tool for synthesizing optically active compounds with high enantiomeric purity.Overall, the diverse applications of N-Ethyl-4-(trifluoromethyl)benzylamine in chemical synthesis highlight its significance as a crucial component in the preparation of advanced materials and bioactive compounds with potential therapeutic benefits.