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Top Quality 2-Naphthyl-beta-D-galactopyranoside 33993-25-8 Hot Sell In Stock
- Molecular Formula: C16H18O6
- Molecular Weight: 306.315
- Appearance/Colour: white to slightly off-white powder
- Melting Point: 196-198 °C
- Boiling Point: 567.9 °C at 760 mmHg
- Flash Point: 297.3 °C
- PSA: 99.38000
- Density: 1.454 g/cm3
- LogP: 0.01850
33993-25-8 Relevant articles
Hierarchical Self-Assembly of a Water-Soluble Organoplatinum(II) Metallacycle into Well-Defined Nanostructures
Datta, Sougata,Saha, Manik Lal,Lahiri, Nabajit,Yu, Guocan,Louie, Janis,Stang, Peter J.
, p. 7020 - 7023 (2018)
A water-soluble metallosupramolecular he...
Structure-based discovery of glycomimetic FmlH ligands as inhibitors of bacterial adhesion during urinary tract infection
Kalas, Vasilios,Hibbing, Michael E.,Maddirala, Amarendar Reddy,Chugani, Ryan,Pinkner, Jerome S.,Mydock-McGrane, Laurel K.,Conover, Matt S.,Janetka, James W.,Hultgren, Scott J.
, p. E2819 - E2828 (2018/03/27)
Treatment of bacterial infections is bec...
Solution and Solid-Phase Stereocontrolled Synthesis of 1,2-cis-Glycopyranosides with Minimally Protected Glycopyranosyl Donors Catalyzed by BF3-N,N-Dimethylformamide Complex
St-Pierre, Gabrielle,Hanessian, Stephen
supporting information, p. 3106 - 3109 (2016/07/14)
Methods are described for the stereosele...
The mechanism of action of beta-galactosidase. Effect of aglycone nature and -deuterium substitution on the hydrolysis of aryl galactosides.
Sinnott,Souchard
, p. 89 - 98 (2007/10/04)
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33993-25-8 Process route
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(2R,3S,4S,5R,6S)-2-(acetoxymethyl)-6-(naphthalen-2-yloxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate
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-
33993-25-8
2-naphthyl-β-D-galactopyranoside
| Conditions | Yield |
|---|---|
|
With
sodium methylate;
In
methanol;
at 20 ℃;
|
100%
|
|
With
methanol; sodium methylate;
|
-
-
C17 H27 BrNO7 PolSi
-
-
108-24-7
acetic anhydride
-
-
135-19-3
β-naphthol
-
-
93218-51-0
2-naphthyl-β-D-galactopyranoside
-
-
33993-25-8
2-naphthyl-β-D-galactopyranoside
| Conditions | Yield |
|---|---|
|
C17H27BrNO7PolSi; β-naphthol;
With
dimethylformamide borontrifluoride;
In
dichloromethane;
at 0 - 20 ℃;
Inert atmosphere;
With
triethylamine hydrofluoride;
In
tetrahydrofuran;
for 3h;
Sealed tube;
acetic anhydride;
With
pyridine;
for 5h;
Overall yield = 100 %; Overall yield = 10 mg; stereoselective reaction;
|
78.947 % de
|
33993-25-8 Upstream products
-
135-19-3
β-naphthol
-
4163-60-4
β-D-galactose peracetate
-
108-24-7
acetic anhydride
-
4451-36-9
2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl chloride
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