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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-Glucose, 2-amino-2-deoxy-, 6-(hydrogen sulfate)

O=C[C@@H]([C@H]([C@@H]([C@@H](COS(=O)(=O)O)O)O)O)N Request for Quotation
Chemical Name: D-Glucose, 2-amino-2-deoxy-, 6-(hydrogen sulfate)
CAS Number: 91674-26-9
Product Number: AG00IGU1(AGN-PC-0VUGDA)
Synonyms:
MDL No: MFCD00063417
Molecular Formula: C6H13NO8S
Molecular Weight: 259.2343

Identification/Properties

Computed Properties
Molecular Weight:
259.229g/mol
XLogP3:
-6.4
Hydrogen Bond Donor Count:
5
Hydrogen Bond Acceptor Count:
9
Rotatable Bond Count:
7
Exact Mass:
259.036g/mol
Monoisotopic Mass:
259.036g/mol
Topological Polar Surface Area:
176A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
311
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
4
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (2R,3S,4R,5R)-5-Amino-2,3,4-trihydroxy-6-oxohexyl hydrogen sulfate plays a crucial role in chemical synthesis as a versatile building block. With its unique structure and functional groups, this compound is widely utilized in the creation of complex organic molecules. Specifically, it serves as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its amino, hydroxyl, and oxo moieties enable it to participate in a range of reactions such as condensation, oxidation, and substitution, facilitating the construction of diverse molecular frameworks. In addition, the sulfated group enhances the compound's solubility and reactivity in aqueous solutions, making it particularly valuable in bioconjugation and medicinal chemistry applications.