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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-Glucopyranose,O-2,3,4,6-tetra-O-acetyl-b-D-glucopyranosyl-(1?4)-O-2,3,6-tri-O-acetyl-b-D-glucopyranosyl-(1?4)-, tetraacetate

CC(=O)OCC1O[C@@H](O[C@@H]2C(COC(=O)C)O[C@H]([C@H]([C@H]2OC(=O)C)OC(=O)C)OC(=O)C)[C@H]([C@H]([C@@H]1O[C@@H]1OC(COC(=O)C)[C@H]([C@@H]([C@@H]1OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C Request for Quotation
Chemical Name: D-Glucopyranose,O-2,3,4,6-tetra-O-acetyl-b-D-glucopyranosyl-(1?4)-O-2,3,6-tri-O-acetyl-b-D-glucopyranosyl-(1?4)-, tetraacetate
CAS Number: 17690-94-7
Product Number: AG0024ZX(AGN-PC-0QB1G0)
Synonyms:
MDL No:
Molecular Formula: C40H54O27
Molecular Weight: 966.8406

Identification/Properties

Computed Properties
Molecular Weight:
966.845g/mol
XLogP3:
-1.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
27
Rotatable Bond Count:
29
Exact Mass:
966.285g/mol
Monoisotopic Mass:
966.285g/mol
Topological Polar Surface Area:
335A^2
Heavy Atom Count:
67
Formal Charge:
0
Complexity:
1850
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
14
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


D-Cellotriose Undecaacetate, a derivative of the natural sugar compound cellotriose, is a versatile molecule widely used in chemical synthesis applications. This compound serves as a valuable building block in the creation of various organic compounds due to its unique chemical properties.One of the primary applications of D-Cellotriose Undecaacetate in chemical synthesis is its role as a precursor for the synthesis of complex carbohydrate-based molecules. By utilizing the functional groups present in D-Cellotriose Undecaacetate, chemists can easily modify and transform this compound into a wide range of derivatives with specific chemical functionalities. These derivatives can then be further utilized in the synthesis of specialized compounds for various industrial and research purposes.Moreover, D-Cellotriose Undecaacetate is often employed in the development of new pharmaceutical drugs and bioactive compounds. Its structural characteristics provide a solid foundation for the creation of drug candidates with enhanced pharmacological properties and bioavailability. By incorporating D-Cellotriose Undecaacetate into the molecular structure of drug molecules, chemists can optimize their efficacy and improve their overall performance in medical applications.Overall, D-Cellotriose Undecaacetate plays a crucial role in chemical synthesis by enabling the efficient construction of complex organic compounds with tailored properties. Its versatility and reactivity make it a valuable asset in the hands of synthetic chemists striving to innovate and advance the field of organic chemistry.