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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-Asparagine, N2-[(1,1-dimethylethoxy)carbonyl]-, 4-nitrophenyl ester

NC(=O)C[C@@H](C(=O)Oc1ccc(cc1)[N+](=O)[O-])NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: L-Asparagine, N2-[(1,1-dimethylethoxy)carbonyl]-, 4-nitrophenyl ester
CAS Number: 4587-33-1
Product Number: AG003CMO(AGN-PC-0OAIRI)
Synonyms:
MDL No:
Molecular Formula: C15H19N3O7
Molecular Weight: 353.3273

Identification/Properties

Properties
MP:
116-118 °C(lit.)
BP:
609.3°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
353.331g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
8
Exact Mass:
353.122g/mol
Monoisotopic Mass:
353.122g/mol
Topological Polar Surface Area:
154A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
516
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


Boc-Asn-ONp is a valuable tool in chemical synthesis, particularly in peptide chemistry. This compound serves as a protected form of asparagine, allowing for controlled and selective reactions to take place during the synthesis of peptides. By incorporating Boc-Asn-ONp into a reaction, chemists can ensure that the asparagine residue remains unaltered until the desired step in the synthesis process. This can help to improve the overall efficiency and success rate of peptide synthesis, as well as allow for the production of complex and diverse peptide sequences. Additionally, Boc-Asn-ONp is known for its stability and compatibility with a variety of reaction conditions, making it a versatile choice for peptide chemists seeking reliable and high-quality results.