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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-Galactopyranose, 2-(acetylamino)-2-deoxy-3-O-b-D-galactopyranosyl-

OC[C@H]1OC(O)[C@@H]([C@H]([C@H]1O)O[C@@H]1O[C@H](CO)[C@@H]([C@@H]([C@H]1O)O)O)NC(=O)C Request for Quotation
Chemical Name: D-Galactopyranose, 2-(acetylamino)-2-deoxy-3-O-b-D-galactopyranosyl-
CAS Number: 20972-29-6
Product Number: AG002KDN(AGN-PC-0QWUNG)
Synonyms:
MDL No:
Molecular Formula: C14H25NO11
Molecular Weight: 383.3484

Identification/Properties

Computed Properties
Molecular Weight:
383.35g/mol
XLogP3:
-4.2
Hydrogen Bond Donor Count:
8
Hydrogen Bond Acceptor Count:
11
Rotatable Bond Count:
5
Exact Mass:
383.143g/mol
Monoisotopic Mass:
383.143g/mol
Topological Polar Surface Area:
198A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
480
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
9
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Acetamido-2-deoxy-3-O-(α-D-galactopyranosyl)-β-D-galactopyranose, commonly known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure and reactivity make it a valuable tool in the creation of complex molecules and functional materials.One key application of $name$ in chemical synthesis is its use as a glycosylation reagent. By selectively activating the anomeric position of the galactosyl moiety, $name$ can facilitate the formation of glycosidic bonds with other carbohydrates or functional groups. This glycosylation reaction is essential in the synthesis of glycoconjugates, natural products, and pharmaceutical compounds.Furthermore, the presence of the acetamido and deoxy groups in $name$ provides additional functionality for further derivatization and modification. These groups can be selectively manipulated to introduce various substituents or protective groups, allowing for precise control over the stereochemistry and regioselectivity of the resulting products.In summary, $name$ is a valuable compound in chemical synthesis, offering a diverse range of applications in the construction of complex molecules and bioactive compounds. Its unique structure and reactivity make it an essential building block for the synthesis of glycoconjugates, natural products, and pharmaceuticals.