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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)-

b-D-Galactopyranosylamine, 2,3,4,6-tetrakis(2,2-dimethylpropanoate)

N[C@@H]1O[C@H](COC(=O)C(C)(C)C)[C@@H]([C@@H]([C@H]1OC(=O)C(C)(C)C)OC(=O)C(C)(C)C)OC(=O)C(C)(C)C Request for Quotation
Chemical Name: b-D-Galactopyranosylamine, 2,3,4,6-tetrakis(2,2-dimethylpropanoate)
CAS Number: 108342-87-6
Product Number: AG00HB63(AGN-PC-0OYBMZ)
Synonyms:
MDL No:
Molecular Formula: C26H45NO9
Molecular Weight: 515.6368

Identification/Properties

Computed Properties
Molecular Weight:
515.644g/mol
XLogP3:
5.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
10
Rotatable Bond Count:
13
Exact Mass:
515.309g/mol
Monoisotopic Mass:
515.309g/mol
Topological Polar Surface Area:
140A^2
Heavy Atom Count:
36
Formal Charge:
0
Complexity:
824
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
5
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#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,3,4,6-Tetra-O-pivaloyl-β-D-galactopyranosylamine is a crucial compound utilized in chemical synthesis, particularly in the field of carbohydrate chemistry. Due to its unique structure and reactivity, this compound plays a significant role as a protecting group in the synthesis of complex carbohydrates.In chemical synthesis, 2,3,4,6-Tetra-O-pivaloyl-β-D-galactopyranosylamine is commonly employed to protect the hydroxyl groups of carbohydrates, specifically galactose moieties. By selectively blocking these hydroxyl groups with pivaloyl groups, the compound allows for the manipulation of other functional groups in the molecule without affecting the galactose residues. This protection strategy facilitates the synthesis of intricate carbohydrate-based molecules with high selectivity and efficiency.Moreover, this versatile compound serves as a building block for the construction of diverse glycoconjugates, glycopeptides, and glycolipids. Its compatibility with a variety of reaction conditions and its stability during synthesis make it an indispensable tool in the creation of new carbohydrate derivatives with tailored properties and functions.Overall, the application of 2,3,4,6-Tetra-O-pivaloyl-β-D-galactopyranosylamine in chemical synthesis enables the controlled modification and assembly of complex carbohydrate structures, paving the way for advancements in drug development, material science, and biochemical research.