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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)-

Asparagine, N2-[(phenylmethoxy)carbonyl]-

O=C(N[C@H](C(=O)O)CC(=O)N)OCc1ccccc1 Request for Quotation
Chemical Name: Asparagine, N2-[(phenylmethoxy)carbonyl]-
CAS Number: 2304-96-3
Product Number: AG002LZ4(AGN-PC-0O82LS)
Synonyms:
MDL No:
Molecular Formula: C12H14N2O5
Molecular Weight: 266.2500

Identification/Properties

Computed Properties
Molecular Weight:
266.253g/mol
XLogP3:
-0.1
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
7
Exact Mass:
266.09g/mol
Monoisotopic Mass:
266.09g/mol
Topological Polar Surface Area:
119A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
339
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


Z-Asn-OH, also known as Z-protected asparagine, plays a crucial role in chemical synthesis as a key building block for peptides and proteins. Its application in solid-phase peptide synthesis involves protecting the asparagine residue to prevent unwanted side reactions during peptide bond formation. By utilizing Z-Asn-OH in peptide synthesis, chemists can selectively control the amino acid sequence and stereochemistry of the final peptide product. Additionally, the Z-protecting group can be easily removed under mild conditions, allowing for subsequent modifications and functionalizations. Due to its versatility and reliability in peptide chemistry, Z-Asn-OH is a valuable tool for the synthesis of bioactive peptides and pharmaceutical compounds.