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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-Glucopyranoside, methyl 4,6-O-(phenylmethylene)-

CO[C@@H]1O[C@H]2CO[C@H](O[C@@H]2[C@H]([C@@H]1O)O)c1ccccc1 Request for Quotation
Chemical Name: b-D-Glucopyranoside, methyl 4,6-O-(phenylmethylene)-
CAS Number: 14155-23-8
Product Number: AG006XKR(AGN-PC-0PQZ7C)
Synonyms:
MDL No:
Molecular Formula: C14H18O6
Molecular Weight: 282.2891

Identification/Properties

Computed Properties
Molecular Weight:
282.292g/mol
XLogP3:
-0.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
2
Exact Mass:
282.11g/mol
Monoisotopic Mass:
282.11g/mol
Topological Polar Surface Area:
77.4A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
319
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
5
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, (4aR,6R,7R,8R,8aS)-6-Methoxy-2-phenylhexahydropyrano[3,2-d][1,3]dioxine-7,8-diol serves as a valuable building block due to its unique structural features. This compound can be utilized as a key intermediate for the creation of complex molecules with specific stereochemical arrangements. Its methoxy and phenyl substituents, along with the dioxine and pyrano rings, offer opportunities for diversification through various functional group transformations. In addition, the presence of multiple chiral centers provides a platform for the creation of enantioenriched compounds, essential in the production of pharmaceuticals, agrochemicals, and other fine chemicals.