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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)-

D-Asparagine, N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-

NC(=O)C[C@H](C(=O)O)NC(=O)OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: D-Asparagine, N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-
CAS Number: 108321-39-7
Product Number: AG007D2H(AGN-PC-0NWWOY)
Synonyms:
MDL No:
Molecular Formula: C19H18N2O5
Molecular Weight: 354.3566

Identification/Properties

Computed Properties
Molecular Weight:
354.362g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
7
Exact Mass:
354.122g/mol
Monoisotopic Mass:
354.122g/mol
Topological Polar Surface Area:
119A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
530
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


Fmoc-D-Asparagine is a versatile amino acid derivative commonly used in chemical synthesis for peptide and protein synthesis. Its unique properties make it a valuable building block in the production of peptide-based drugs, natural product synthesis, and materials science research. By incorporating Fmoc-D-Asparagine into peptide chains, chemists can control the structure, stability, and functionality of the resulting molecules, enabling precise manipulation of biological activity and properties. Additionally, Fmoc-D-Asparagine's compatibility with solid-phase peptide synthesis techniques enhances efficiency and yields in the production of complex peptide sequences. Its widespread applications in the pharmaceutical and biotechnology industries highlight its significance as a key component in the synthesis of bioactive compounds.