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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)-

(S)-1-(tert-Butoxycarbonyl)-5-oxopiperazine-2-carboxylic acid

O=C1NC[C@H](N(C1)C(=O)OC(C)(C)C)C(=O)O Request for Quotation
Chemical Name: (S)-1-(tert-Butoxycarbonyl)-5-oxopiperazine-2-carboxylic acid
CAS Number: 1033713-11-9
Product Number: AG009123(AGN-PC-0WA2T8)
Synonyms:
MDL No:
Molecular Formula: C10H16N2O5
Molecular Weight: 244.2444

Identification/Properties

Computed Properties
Molecular Weight:
244.247g/mol
XLogP3:
-0.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
244.106g/mol
Monoisotopic Mass:
244.106g/mol
Topological Polar Surface Area:
95.9A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
347
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


(S)-1-(tert-Butoxycarbonyl)-5-oxopiperazine-2-carboxylic acid, also known as Boc-Glu-OPfp, is a valuable compound widely utilized in chemical synthesis, particularly in peptide synthesis and pharmaceutical drug development. It serves as a key building block in the creation of peptide sequences due to its ability to protect the glutamic acid residue during peptide assembly.This compound functions as a versatile intermediate in organic chemistry, enabling the selective modification of amino acids and peptides. Through its Boc (tert-butoxycarbonyl) protecting group, it shields the carboxyl group of glutamic acid, preventing unwanted reactions during peptide chain elongation. By incorporating (S)-1-(tert-Butoxycarbonyl)-5-oxopiperazine-2-carboxylic acid into peptide synthesis, chemists can precisely control the sequence and structure of peptides, essential for the development of bioactive molecules and pharmaceuticals.Furthermore, the use of (S)-1-(tert-Butoxycarbonyl)-5-oxopiperazine-2-carboxylic acid in chemical synthesis allows for the creation of complex peptide-based scaffolds for drug discovery and medicinal chemistry. Its strategic incorporation enables the generation of diverse peptide derivatives with unique properties, facilitating drug optimization and enhancing therapeutic potential.Overall, (S)-1-(tert-Butoxycarbonyl)-5-oxopiperazine-2-carboxylic acid plays a crucial role in the synthesis of peptides and peptide-based compounds, offering chemists a powerful tool for designing and developing novel pharmaceutical agents and bioactive molecules.