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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)-

L-Lysine, N2-[(1,1-dimethylethoxy)carbonyl]-N6-(trifluoroacetyl)-

O=C(OC(C)(C)C)N[C@H](C(=O)O)CCCCNC(=O)C(F)(F)F Request for Quotation
Chemical Name: L-Lysine, N2-[(1,1-dimethylethoxy)carbonyl]-N6-(trifluoroacetyl)-
CAS Number: 16965-06-3
Product Number: AG00APCY(AGN-PC-0O4STI)
Synonyms:
MDL No:
Molecular Formula: C13H21F3N2O5
Molecular Weight: 342.3114

Identification/Properties

Computed Properties
Molecular Weight:
342.315g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
9
Exact Mass:
342.14g/mol
Monoisotopic Mass:
342.14g/mol
Topological Polar Surface Area:
105A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
432
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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


N2-Boc-N6-(2,2,2-trifluoroacetyl)-L-lysine is a valuable compound widely utilized in chemical synthesis, particularly in the field of peptide synthesis. With its unique structural and chemical properties, this compound serves as a versatile building block for the creation of complex peptides and proteins.In chemical synthesis, N2-Boc-N6-(2,2,2-trifluoroacetyl)-L-lysine plays a crucial role as a protecting group. By selectively shielding the amine and carboxyl functional groups of lysine, this compound enables precise control over sequential peptide bond formations. This protection strategy allows chemists to manipulate specific reactive sites within a peptide chain, facilitating the stepwise assembly of intricate peptide sequences with high purity and yield.Furthermore, the trifluoroacetyl group attached to the lysine side chain enhances the hydrophobicity and stability of the peptide product. This modification can influence the physicochemical properties of the synthesized peptide, making it suitable for various applications in drug discovery, protein engineering, and biochemical research.Overall, the strategic incorporation of N2-Boc-N6-(2,2,2-trifluoroacetyl)-L-lysine in chemical synthesis enables the efficient and controlled construction of diverse peptide structures, opening up new possibilities for the development of novel bioactive molecules and functional materials.