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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-Glucopyranose, 1,6-anhydro-, triacetate

CC(=O)O[C@H]1[C@H](OC(=O)C)[C@H]2CO[C@@H]([C@@H]1OC(=O)C)O2 Request for Quotation
Chemical Name: b-D-Glucopyranose, 1,6-anhydro-, triacetate
CAS Number: 13242-55-2
Product Number: AG0010OV(AGN-PC-0PJQ2B)
Synonyms:
MDL No:
Molecular Formula: C12H16O8
Molecular Weight: 288.2506

Identification/Properties

Computed Properties
Molecular Weight:
288.252g/mol
XLogP3:
-0.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
6
Exact Mass:
288.085g/mol
Monoisotopic Mass:
288.085g/mol
Topological Polar Surface Area:
97.4A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
420
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The β-D-Glucopyranose, 1,6-anhydro-, 2,3,4-triacetate plays a crucial role in chemical synthesis as a versatile building block. Its unique structure and reactivity make it an excellent starting material for the synthesis of various complex organic molecules. This compound can be utilized as a protecting group for hydroxyl functionalities in organic synthesis, allowing for selective reactions at specific sites within a molecule. Additionally, its triacetyl moiety can serve as a handle for further functionalization, enabling the attachment of different chemical groups to tailor the properties of the final product. By leveraging the properties of this compound, chemists can efficiently access a diverse array of structurally complex and biologically active compounds through strategic synthetic pathways.