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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)-

(2R,4S,5R,6R)-5-acetamido-4-hydroxy-2-(4-nitrophenoxy)-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid

OC[C@H]([C@H]([C@@H]1O[C@@](C[C@@H]([C@H]1NC(=O)C)O)(Oc1ccc(cc1)[N+](=O)[O-])C(=O)O)O)O Request for Quotation
Chemical Name: (2R,4S,5R,6R)-5-acetamido-4-hydroxy-2-(4-nitrophenoxy)-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid
CAS Number: 26112-88-9
Product Number: AG002RPK(AGN-PC-0426AZ)
Synonyms:
MDL No: MFCD00132944
Molecular Formula: C17H22N2O11
Molecular Weight: 430.3634

Identification/Properties

Computed Properties
Molecular Weight:
430.366g/mol
XLogP3:
-1.3
Hydrogen Bond Donor Count:
6
Hydrogen Bond Acceptor Count:
11
Rotatable Bond Count:
7
Exact Mass:
430.122g/mol
Monoisotopic Mass:
430.122g/mol
Topological Polar Surface Area:
212A^2
Heavy Atom Count:
30
Formal Charge:
0
Complexity:
634
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
6
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


2-O-(p-Nitrophenyl)-α-D-N-acetylneuraminic acid, also known as p-nitrophenyl sialic acid, is a versatile compound commonly used in chemical synthesis for various applications. This compound serves as a key building block in the synthesis of glycoconjugates, specifically in the construction of glycoproteins and glycolipids. Its functional groups enable precise modification and manipulation, allowing chemists to introduce specific chemical moieties or linkers for targeted applications. Additionally, the presence of the acetyl group provides a site for further derivatization, broadening the scope of its utility in synthetic chemistry.Furthermore, the nitrophenyl group can serve as a convenient protecting group, aiding in the selective deprotection of certain functional groups during complex synthetic processes. Its stability under a range of conditions makes it a valuable tool for chemists seeking to perform controlled chemical transformations.Overall, the strategic placement of functional groups in 2-O-(p-Nitrophenyl)-α-D-N-acetylneuraminic acid makes it an essential compound for chemists involved in the synthesis of bioactive molecules, pharmaceutical intermediates, and other complex organic compounds. Its versatility and compatibility with various synthetic methodologies make it a valuable asset in the toolkit of synthetic chemists.