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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-fluoro-

CCNCc1ccc(cc1)F Request for Quotation
Chemical Name: Benzenemethanamine, N-ethyl-4-fluoro-
CAS Number: 162401-03-8
Product Number: AG001T2E(AGN-PC-0LG00Y)
Synonyms:
MDL No: MFCD04537942
Molecular Formula: C9H12FN
Molecular Weight: 153.1967

Identification/Properties

Properties
BP:
197.3°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
153.2g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
153.095g/mol
Monoisotopic Mass:
153.095g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
97.7
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-Ethyl-4-fluorobenzylamine is a versatile compound commonly used in chemical synthesis as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. This compound serves as a crucial building block in the synthesis of complex organic molecules due to its unique structure and reactivity.In organic synthesis, N-Ethyl-4-fluorobenzylamine can be employed as a starting material for the preparation of a wide range of functionalized benzylamines, which are important structural motifs in numerous bioactive compounds. Its ability to undergo various transformations, such as nucleophilic substitution, reductive amination, and cross-coupling reactions, makes it a valuable precursor in the synthesis of diverse chemical entities.Furthermore, the presence of the ethyl group enhances the lipophilicity and solubility of N-Ethyl-4-fluorobenzylamine, making it particularly useful in designing new drug candidates with improved pharmacokinetic properties. This compound's versatility and synthetic utility make it a valuable tool for medicinal chemists, agrochemists, and researchers working in the field of organic synthesis.