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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)-

(2R,3R,4S,5R)-2-(hydroxymethyl)-6-naphthalen-2-yloxyoxane-3,4,5-triol

OCC1O[C@H](Oc2ccc3c(c2)cccc3)C([C@@H]([C@@H]1O)O)O C16H18O6 Request for Quotation
Chemical Name: (2R,3R,4S,5R)-2-(hydroxymethyl)-6-naphthalen-2-yloxyoxane-3,4,5-triol
CAS Number: 25320-79-0
Product Number: AG00I4U4(AGN-PC-00UR6E)
Synonyms:
MDL No: MFCD00067170
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
306.314g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
3
Exact Mass:
306.11g/mol
Monoisotopic Mass:
306.11g/mol
Topological Polar Surface Area:
99.4A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
365
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H319-H315-H335
Precautionary Statements:
P261-P342+P311-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (2R,3S,4S,5R,6R)-2-(Hydroxymethyl)-6-(naphthalen-2-yloxy)tetrahydro-2H-pyran-3,4,5-triol has proven to be a valuable component in chemical synthesis due to its unique structural properties. This compound serves as a versatile building block in the creation of complex molecules, particularly in the field of organic chemistry. Its hydroxyl groups allow for the formation of various bonds and interactions with other molecules, facilitating the construction of intricate chemical structures. Additionally, the presence of the naphthalen-2-yloxy group introduces aromaticity, providing additional reactivity and selectivity in chemical reactions. Overall, this compound plays a crucial role in the design and synthesis of novel compounds with potential applications in pharmaceuticals, materials science, and other areas of research.