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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)-

a-D-Glucopyranoside, 1,3,4,6-tetra-O-acetyl-b-D-fructofuranosyl,tetraacetate

CC(=O)OC[C@@]1(O[C@H]2O[C@H](COC(=O)C)[C@H]([C@@H]([C@H]2OC(=O)C)OC(=O)C)OC(=O)C)O[C@@H]([C@H]([C@@H]1OC(=O)C)OC(=O)C)COC(=O)C Request for Quotation
Chemical Name: a-D-Glucopyranoside, 1,3,4,6-tetra-O-acetyl-b-D-fructofuranosyl,tetraacetate
CAS Number: 126-14-7
Product Number: AG000QO9(AGN-PC-0PI7W4)
Synonyms:
MDL No:
Molecular Formula: C28H38O19
Molecular Weight: 678.5899

Identification/Properties

Computed Properties
Molecular Weight:
678.593g/mol
XLogP3:
-0.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
19
Rotatable Bond Count:
21
Exact Mass:
678.201g/mol
Monoisotopic Mass:
678.201g/mol
Topological Polar Surface Area:
238A^2
Heavy Atom Count:
47
Formal Charge:
0
Complexity:
1210
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
9
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


Sucrose octaacetate is a versatile compound commonly used in chemical synthesis as an acetylation reagent. It serves as a chemical intermediate in the synthesis of various organic compounds, including flavors, fragrances, and pharmaceuticals. Due to its high reactivity and specificity in acetylation reactions, sucrose octaacetate is often employed to selectively modify hydroxyl groups in a wide range of substrates. This compound plays a crucial role in the production of specialized derivatives for applications such as food additives, artificial sweeteners, and medicinal products. Additionally, sucrose octaacetate's unique properties make it a valuable tool in research and development, enabling the creation of new and innovative molecules with tailored properties and functions.