7306-64-1

Basic information

• Product Name: 6-(2,2-DIMETHYL-[1,3]DIOXOLAN-4-YL)-2,2-DIMETHYL-DIHYDRO-FURO[3,4-D][1,3]DIOXOL-4-ONE
• Synonyms: 6-(2,2-DIMETHYL-[1,3]DIOXOLAN-4-YL)-2,2-DIMETHYL-DIHYDRO-FURO[3,4-D][1,3]DIOXOL-4-ONE;2,3:5,6-Di-O-isopropylidene-L-gulono-1,4-lactone;2,3:5,6-Bis-O-(1-Methylethylidene)-L-gulonic Acid γ-Lactone;5, 6-di-O-isopropylidene- L-gulono-1,4-lactone
• CAS NO: 7306-64-1
• Molecular Formula: C₁₂H₁₈O₆
• Molecular Weight: 258.27
• Product Categories: 13C & 2H Sugars;Carbohydrates & Derivatives
• Mol File: 7306-64-1.mol
• Article Data: 35

Chemical Properties

• Melting Point: 147-149°C
• Boiling Point: 361.2±42.0 °C(Predicted)
• Appearance: /
• Density: 1 +-.0.06 g/cm3(Predicted)
• Storage Temp.: -20°C Freezer
• Solubility: Acetone, Dichloromethane, Methanol
• CAS DataBase Reference: 6-(2,2-DIMETHYL-[1,3]DIOXOLAN-4-YL)-2,2-DIMETHYL-DIHYDRO-FURO[3,4-D][1,3]DIOXOL-4-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(2,2-DIMETHYL-[1,3]DIOXOLAN-4-YL)-2,2-DIMETHYL-DIHYDRO-FURO[3,4-D][1,3]DIOXOL-4-ONE(7306-64-1)
• EPA Substance Registry System: 6-(2,2-DIMETHYL-[1,3]DIOXOLAN-4-YL)-2,2-DIMETHYL-DIHYDRO-FURO[3,4-D][1,3]DIOXOL-4-ONE(7306-64-1)

Safety Data

• Hazardous Substances Data: 7306-64-1(Hazardous Substances Data)

Usage

Description

6-(2,2-DIMETHYL-[1,3]DIOXOLAN-4-YL)-2,2-DIMETHYL-DIHYDRO-FURO[3,4-D][1,3]DIOXOL-4-ONE is a complex organic compound characterized by its unique chemical structure, which includes dioxolan and dihydrofuran moieties. As a white crystalline solid, it possesses distinct chemical properties that make it suitable for various applications in different industries.

Uses

Used in Pharmaceutical Industry:
6-(2,2-DIMETHYL-[1,3]DIOXOLAN-4-YL)-2,2-DIMETHYL-DIHYDRO-FURO[3,4-D][1,3]DIOXOL-4-ONE is used as a synthetic intermediate for the development of novel pharmaceutical compounds. Its unique structure allows for the creation of new drugs with potential therapeutic applications.
Used in Chemical Synthesis:
In the field of chemical synthesis, 6-(2,2-DIMETHYL-[1,3]DIOXOLAN-4-YL)-2,2-DIMETHYL-DIHYDRO-FURO[3,4-D][1,3]DIOXOL-4-ONE serves as a valuable building block for the synthesis of more complex molecules. Its versatile structure can be further modified to create a wide range of compounds with diverse properties and applications.
Used in Material Science:
6-(2,2-DIMETHYL-[1,3]DIOXOLAN-4-YL)-2,2-DIMETHYL-DIHYDRO-FURO[3,4-D][1,3]DIOXOL-4-ONE can be utilized in the development of new materials with specific properties, such as improved stability, reactivity, or selectivity. Its incorporation into polymers or other materials can lead to enhanced performance in various applications.
Used in Carbohydrate Synthesis:
6-(2,2-DIMETHYL-[1,3]DIOXOLAN-4-YL)-2,2-DIMETHYL-DIHYDRO-FURO[3,4-D][1,3]DIOXOL-4-ONE is used as a synthetic intermediate for carbohydrate synthesis. Its unique structure allows for the creation of complex carbohydrate derivatives with potential applications in various industries, such as pharmaceuticals, food, and cosmetics.

Upstream product

• 14131-84-1 2,3:5,6-di-O-isopropylidene-α-D-mannofuranose 
• 7757-38-2 2,3,5,6-di-O-isopropylidene-D-mannofuranose 
• 3458-28-4 D-Mannose 
• 7757-38-2 2,3:5,6-di-O-isopropylidene-α-D-mannofuranose 
• 159423-92-4 (R)-3-{(4R,5R)-5-[(R)-Acetoxy-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-methyl]-2,2-dimethyl-[1,3]dioxolan-4-yl}-2-diazo-3-hydroxy-propionic acid ethyl ester 
• 159423-91-3 4-O-acetyl-2,3:5,6-di-O-isopropylidene-aldehydo-D-mannose 
• 77-76-9 2,2-dimethoxy-propane 
• 1128-23-0 L-gulonolactone 
• 7757-38-2 O²,O³,O⁵,O⁶-diisopropylidene D-mannofuranose 
• 67-64-1 acetone 
• 530-26-7 D-Mannose 
• 40036-82-6 [2,3:5,6]-di-O-isopropylidene-D-mannose 
• 95517-29-6 1-C-nitroso-2,3:5,6-di-O-isopropylidenemannofurasonyl chloride 
• 131444-81-0 5-O-acetyl-1,2-dideoxy-3,4:6,7-di-O-isopropylidene-D-manno-hept-1-enitol 

Downstream Products

• 630390-63-5 (4R)-4-[(4'R)-1'-O-acetyl-2',3'-O-isopropylidene-L-erythrofuranos-4'-yl]-2-phenylamino-2-oxazoline 
• 630390-56-6 1-O-acetyl-2,3-O-isopropylidene-6-O-trityl-β-L-gulofuranose 
• 630390-57-7 1-O-acetyl-5-azido-5-deoxy-2,3-O-isopropylidene-6-O-trityl-α-D-mannofuranose 
• 329010-28-8 (4R,5R)-4-(tert-butyldiphenylsilanoxy)-5-[octa-2(Z),5(E)-dienyl]-tetrahydrofuran-2-one 
• 550316-70-6 (4R,5R)-4-(tert-butyldiphenylsilanyloxy)-5-vinyl-tetrahydrofuran-2-one 
• 445412-03-3 (3aS,6S,6aS)-6-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-dihydro-furo[3,4-d][1,3]dioxol-4-one O-benzyl-oxime 
• 64487-91-8 2-C-hydroxymethyl-2,3:5,6-di-O-isopropylidene-L-gulono-1,4-lactone 

Relevant articles and documents

Dimerization of aldosuloses and aldonolactones into branched higher carbon sugars

Homo-dimerizations of a variety of aldosulose and aldonolactone derivatives via aldol and Claisen reactions have been achieved, leading to novel branched higher carbon sugars in a highly stereoselective manner.

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