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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-Glucose,O-a-D-galactopyranosyl-(1?6)-O-a-D-galactopyranosyl-(1?6)-

O=C[C@@H]([C@H]([C@@H]([C@@H](CO[C@H]1O[C@H](CO[C@H]2O[C@H](CO)[C@@H]([C@@H]([C@H]2O)O)O)[C@@H]([C@@H]([C@H]1O)O)O)O)O)O)O Request for Quotation
Chemical Name: D-Glucose,O-a-D-galactopyranosyl-(1?6)-O-a-D-galactopyranosyl-(1?6)-
CAS Number: 13382-86-0
Product Number: AG009BJL(AGN-PC-0PK4VL)
Synonyms:
MDL No:
Molecular Formula: C18H32O16
Molecular Weight: 504.4371

Identification/Properties

Computed Properties
Molecular Weight:
504.438g/mol
XLogP3:
-7.2
Hydrogen Bond Donor Count:
11
Hydrogen Bond Acceptor Count:
16
Rotatable Bond Count:
11
Exact Mass:
504.169g/mol
Monoisotopic Mass:
504.169g/mol
Topological Polar Surface Area:
277A^2
Heavy Atom Count:
34
Formal Charge:
0
Complexity:
625
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
14
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


Manninotriose is a unique carbohydrate compound that holds significant value in chemical synthesis applications. This trisaccharide, composed of three mannose units linked together, serves as a building block in the creation of various complex molecules. Its intricate structure and functional groups make it ideal for facilitating organic reactions and forming diverse chemical bonds. In chemical synthesis, Manninotriose can be leveraged as a key intermediate for producing pharmaceuticals, natural products, and other specialized compounds. By harnessing the reactivity and versatility of Manninotriose, chemists can achieve precise control over reaction pathways and efficiently craft intricate molecular structures with tailored properties.