42926-89-6

Basic information

• Product Name: 1,2-O-isopropylidene-3-O-benzyl-α-D-glucofuranose
• Synonyms: 1,2-O-isopropylidene-3-O-benzyl-α-D-glucofuranose
• CAS NO: 42926-89-6
• Molecular Weight: 310.347
• Mol File: 42926-89-6.mol
• Article Data: 17

Chemical Properties

• CAS DataBase Reference: 1,2-O-isopropylidene-3-O-benzyl-α-D-glucofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-O-isopropylidene-3-O-benzyl-α-D-glucofuranose(42926-89-6)
• EPA Substance Registry System: 1,2-O-isopropylidene-3-O-benzyl-α-D-glucofuranose(42926-89-6)

Safety Data

• Hazardous Substances Data: 42926-89-6(Hazardous Substances Data)

Usage

Class

Glucopyranose derivatives

Explanation

1,2-O-isopropylidene-3-O-benzyl-α-D-glucofuranose belongs to the class of glucopyranose derivatives, which are compounds derived from α-D-glucose.

Explanation

The compound is a derivative of α-D-glucose, a monosaccharide that serves as the parent molecule for this specific compound.

Explanation

The isopropylidene group is a chemical modification that is attached to the 1 and 2 positions of the glucose molecule, contributing to the compound's structure and properties.

Explanation

The benzyl group is another chemical modification attached to the 3 position of the glucose molecule, further defining the compound's structure and properties.

Explanation

1,2-O-isopropylidene-3-O-benzyl-α-D-glucofuranose is used in organic chemistry for the synthesis of other carbohydrate derivatives and in medicinal chemistry for the development of potential drug candidates.

Explanation

The presence of the isopropylidene and benzyl groups in the compound allows for various chemical reactions and modifications, making it a valuable building block in organic synthesis.

Explanation

The compound is a modified version of α-D-glucofuranose, a five-membered ring form of α-D-glucose, with additional functional groups attached to specific positions on the ring.

Parent compound

α-D-glucose

Isopropylidene group

Attached at positions 1 and 2

Benzyl group

Attached at position 3

Applications

Organic chemistry and medicinal chemistry

Chemical reactivity

Enabled by isopropylidene and benzyl groups

Structure

Modified α-D-glucofuranose

Upstream product

• 50-99-7 D-glucose 
• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 37776-15-1 6-O-Benzoyl-3-O-benzyl-1,2-O-isopropylidene-α-D-glucofuranose 
• 134198-40-6 6-O-benzoyl-3-O-benzyl-1,2-O-isopropylidene-5-O-methanesulfonyl-α-D-glucofuranose 
• 591727-19-4 1-2,5-6 di-O-isopropylidene 3-O-benzyl α(D)gluco-pentoaldofuranose 
• 350255-13-9 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 1207730-45-7 3-O-benzyl-1,2-O-isopropylidene-6-O-(2,4,6-triisopropylbenzoyl)-β-L-idofuranose 
• 100-39-0 benzyl bromide 
• 582-52-5 1,2:5,6-diacetone-D-glucose 
• 84563-90-6 6-O-acetyl-3-O-benzyl-1,2-O-isopropylidene-5-O-methanesulfonyl-α-D-glucofuranose 
• 18006-25-2 3-O-benzyl-1,2-O-isopropylidene-α-D-glucofuranose diacetate 
• 18685-18-2 3-O-benzyl-1,2-5,6-O-diisopropylidene-α-D-glucofuranose 
• 22331-19-7 3-O-benzyl-1,2-O-isopropylidene-5,6-di-O-mesyl-α-D-glucofuranose 
• 23558-05-6 3-O-benzyl-1,2-O-isopropylidene-1,5-D-xylo-dialdofuranose 

Downstream Products

• 1439518-81-6 C₂₅H₂₆O₅S 
• 1439516-36-5 C₂₅H₂₉BrO₅S 
• 1439516-28-5 C₂₅H₂₇BrO₅S 
• 23313-03-3 (R)-2-[(3aR,5R,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]-2-hydroxyethyl 4-methylbenzenesulfonate 
• 23313-05-5 6-azido-3-O-benzyl-6-deoxy-1,2-O-(1-methylethylidene)-α-D-glucofuranose 
• 23567-05-7 1,6-Anhydro-2,3,4-tri-O-benzoyl-β-D-glucopyranose 
• 498-07-7 levoglucosan 
• 66963-60-8 1,6-anhydro-3-O-benzyl-β-D-glucopyranose 
• 882689-03-4 Benzoic acid (S)-2-((3aR,5S,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-2-methanesulfonyloxy-ethyl ester 

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