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- High Purity Sucrose Ester Of Fatty Acids
- Sucrose Ester Of Fatty Acids S-CM
- Sucrose Ester Of Fatty Acids
- Compound Food Additive
- 2,3,4,6-Tetra-O-Benzyl-D-Glucopyranose
- 2,3,4,6-Tetra-O-Benzyl-D-Galactose
- Mono-Acetone-D-Glucose
- Diacetone-D-Glucose
- Methyl?α-D-Mannopyranoside
- 1,2,3,4-Tetra-O-acetyl-β-D-glucuronic acid methyl ester
Carbohydrate Derivative
METHYL 4,6-O-BENZYLIDENE- α-D-GLUCOPYRANOSIDE
NAME：METHYL 4,6-O-BENZYLIDENE- α-D-GLUCOPYRANOSIDE
CAS No.：3162-96-7
Molecular Formula:：C14H18O6
Molecular Weight：282.29
EINECS號：221-615-2
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Quality Standard:
| Item | Specification |
| Appearance | White to off-white crystalline powder |
| Assay , % | ≥98.0 |
| Melting point, ℃ | 160.0~167.0 |
| Specific rotation [α]20D (C=1,CHCl3) | +108.5~ +114.5° |
| Loss on drying, % | ≤1.0 |
| Residue on ignition, % | ≤0.10 |
USES:
- Methyl-4, 6-benzylidene -α -D-glucopyranoside is a commonly used benzylidene protected carbohydrate derivative, usually as an intermediate, widely used in the synthesis of a variety of compounds.
The specific application is described as follows:
- By synthesizing a deacetyllanatoside glucosyl-modified compound (2-O-benzyl-beta-D-glucopyranoside-deacetyllanatoside and the like) to enhance the antitumous effect of the compound, the potency is improved, the half-life period is prolonged, meanwhile, the modified compound is prepared into a liposome, the hepatic targeting effect of the liposome is improved, and the cardiotoxicity is reduced.
- It is used for the construction of chiral trifluoromethylated quaternary carbon centres
- Synthesis of new C-6 homologues of 1-deoxynojirimycin and 1-deoxy- L –idonojirimycin.
- Use of Propargyl Glycoside for Anomeric Protection
- Synthesis of phenylurethane.
- It is used for synthesis and antimicrobial studies of pyranmycin.
- Synthesis of several Alkyl Hex-3-enopyranosiduloses.
- This product reacts with dibromomethane in aqueous solution of sodium hydroxide, using tetrabutylammonium bromide as phase transfer agent, can obtain corresponding 2, 3-methylene acetal. This product protects the 4th and 6th positions
- This product can be oxidated and ring opened by n-bromosuccinimide (NBS), and generate 6-bromo-4-O-benzoyl pyranhexose.
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