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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)-

Carbamic acid,[(1S)-1-[[(4-methyl-2-oxo-2H-1-benzopyran-7-yl)amino]carbonyl]-5-[(trifluoroacetyl)amino]pentyl]-, 1,1-dimethylethyl ester

O=C(OC(C)(C)C)N[C@H](C(=O)Nc1ccc2c(c1)oc(=O)cc2C)CCCCNC(=O)C(F)(F)F Request for Quotation
Chemical Name: Carbamic acid,[(1S)-1-[[(4-methyl-2-oxo-2H-1-benzopyran-7-yl)amino]carbonyl]-5-[(trifluoroacetyl)amino]pentyl]-, 1,1-dimethylethyl ester
CAS Number: 97885-44-4
Product Number: AG01E6HG(AGN-PC-0W7N7W)
Synonyms:
MDL No: MFCD11975034
Molecular Formula: C23H28F3N3O6
Molecular Weight: 499.4801296

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Chemical Structure


Boc-Lys(Tfa)-AMC is a versatile compound commonly utilized in chemical synthesis for the preparation of peptide and protein molecules. This specially designed reagent plays a crucial role in the protection and manipulation of amino acid residues during the synthesis process. By incorporating this compound into a reaction, chemists can selectively introduce a Boc (tert-butoxycarbonyl) protecting group onto the lysine amino acid, enabling precise control over subsequent modifications.In peptide synthesis, Boc-Lys(Tfa)-AMC serves as a key building block for constructing peptide chains with high accuracy and efficiency. The Boc protecting group shields the amino group of lysine, preventing unwanted side reactions and ensuring the desired chemical transformations occur at the intended sites. Additionally, the trifluoroacetyl (Tfa) moiety offers stability and compatibility with a wide range of synthetic conditions, further enhancing the versatility of this reagent in peptide chemistry.Through strategic incorporation of Boc-Lys(Tfa)-AMC into synthetic pathways, chemists can streamline the assembly of complex peptides and proteins with precise control over protecting group strategy. This compound facilitates the synthesis of custom-designed biomolecules for a variety of applications in pharmaceuticals, biotechnology, and materials science. Its strategic role in chemical synthesis highlights its importance as a valuable tool for creating tailored peptides with specific functionalities and structures.