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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)-

1-[(2-methylpropan-2-yl)oxycarbonyl]-4-phenylmethoxycarbonylpiperazine-2-carboxylic acid

OC(=O)C1CN(CCN1C(=O)OC(C)(C)C)C(=O)OCc1ccccc1 Request for Quotation
Chemical Name: 1-[(2-methylpropan-2-yl)oxycarbonyl]-4-phenylmethoxycarbonylpiperazine-2-carboxylic acid
CAS Number: 149057-19-2
Product Number: AG00HXOI(AGN-PC-0KKLAI)
Synonyms:
MDL No:
Molecular Formula: C18H24N2O6
Molecular Weight: 364.3930

Identification/Properties

Computed Properties
Molecular Weight:
364.398g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
6
Exact Mass:
364.163g/mol
Monoisotopic Mass:
364.163g/mol
Topological Polar Surface Area:
96.4A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
524
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


1-Boc-4-Cbz-2-piperazinecarboxylic acid is a versatile compound widely used in chemical synthesis as a key building block for the preparation of various organic compounds. With its unique structural properties, this compound serves as a crucial intermediate in the synthesis of pharmaceuticals, agrochemicals, and functional materials.In chemical synthesis, 1-Boc-4-Cbz-2-piperazinecarboxylic acid plays a vital role as a protecting group, facilitating selective reactions by temporarily masking certain functional groups on other molecules. This protective strategy enables chemists to manipulate specific sites within complex molecular structures without affecting the overall reactivity of the compounds involved.Furthermore, 1-Boc-4-Cbz-2-piperazinecarboxylic acid is commonly utilized in the construction of peptidomimetics and peptide-based drugs due to its ability to introduce the Boc (tert-butoxycarbonyl) and Cbz (benzyloxycarbonyl) protecting groups onto amino acid residues. This protective function is essential for the controlled assembly of peptide chains and the synthesis of bioactive molecules with enhanced stability and bioavailability.Overall, the strategic incorporation of 1-Boc-4-Cbz-2-piperazinecarboxylic acid in chemical synthesis enables precise and efficient molecular transformations, paving the way for the development of novel compounds with diverse applications in the fields of pharmaceuticals, agrochemicals, and materials science.