33208-47-8

Basic information

• Product Name: .beta.-D-Mannopyranose, 1,6:2,3-dianhydro-4-O-(phenylmethyl)-
• Synonyms: .beta.-D-Mannopyranose, 1,6:2,3-dianhydro-4-O-(phenylmethyl)-;1,6:2,3-Dianhydro-4-O-benzyl-beta-D-mannopyranose min. 99%;1,6:2,3-Dianhydro-4-O-benzyl-beta-D-mannopyranose
• CAS NO: 33208-47-8
• Molecular Formula: C₁₃H₁₄O₄
• Molecular Weight: 234.24786
• Mol File: 33208-47-8.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: .beta.-D-Mannopyranose, 1,6:2,3-dianhydro-4-O-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: .beta.-D-Mannopyranose, 1,6:2,3-dianhydro-4-O-(phenylmethyl)-(33208-47-8)
• EPA Substance Registry System: .beta.-D-Mannopyranose, 1,6:2,3-dianhydro-4-O-(phenylmethyl)-(33208-47-8)

Safety Data

• Hazardous Substances Data: 33208-47-8(Hazardous Substances Data)

Usage

Description

.beta.-D-Mannopyranose, 1,6:2,3-dianhydro-4-O-(phenylmethyl)is a modified form of mannose, a simple sugar with a six-membered ring structure known as a pyranose form. The modification includes a dianhydro ring formation between the 1st and 6th carbon atoms, and the 2nd and 3rd carbon atoms, with a phenylmethyl group attached to the 4th carbon atom. This unique structure may provide specific properties and reactivity, making it suitable for various applications in the medicinal and industrial fields.

Uses

Used in Pharmaceutical Industry:
.beta.-D-Mannopyranose, 1,6:2,3-dianhydro-4-O-(phenylmethyl)is used as a key component in the development of pharmaceutical compounds due to its unique chemical structure. The modification of the mannose molecule may enhance its interaction with biological targets, potentially leading to the development of new drugs with improved efficacy and selectivity.
Used in Chemical Synthesis:
In the field of chemical synthesis, .beta.-D-Mannopyranose, 1,6:2,3-dianhydro-4-O-(phenylmethyl)can be used as a starting material or intermediate for the synthesis of complex organic molecules. The presence of the phenylmethyl group and the dianhydro ring formation may facilitate specific chemical reactions, allowing for the creation of novel compounds with diverse applications.
Used in Material Science:
The unique structure of .beta.-D-Mannopyranose, 1,6:2,3-dianhydro-4-O-(phenylmethyl)may also find applications in material science, where it could be used to develop new materials with specific properties. For example, its incorporation into polymers could result in materials with enhanced mechanical strength, thermal stability, or biological compatibility.
Used in Research and Development:
As a novel chemical entity, .beta.-D-Mannopyranose, 1,6:2,3-dianhydro-4-O-(phenylmethyl)can be utilized in research and development to explore its potential applications and properties. This may include studies on its biological activity, chemical reactivity, and potential use in various industries, such as pharmaceuticals, chemical synthesis, and material science.

Upstream product

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• 3868-03-9 1,6:2,3-dianhydro-β-D-mannopyranose 
• 100-39-0 benzyl bromide 
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• 13265-84-4 D-glucal 
• 50705-28-7 1,6-anhydro-3,4-dideoxy-β-D-threo-hex-3-enopyranose 
• 161365-77-1 1,6-anhydro-2-chloro-β-D-erythro-hex-3-enopyranose 
• 58394-31-3 1,6-anhydro-2,3-dideoxy-β-D-erythro-hex-2-enopyranose 
• 148473-54-5 Acetic acid (1R,2R,3S,4R,5R)-2-benzyloxy-4-bromo-6,8-dioxa-bicyclo[3.2.1]oct-3-yl ester 
• 2873-29-2 D-glucal triacetate 
• 20183-65-7 1,6-anhydro-4-O-benzyl-2-O-(4-toluenesulfonyl)-β-D-glucopyranose 
• 50767-55-0 1,6-anhydro-4-O-benzyl-2-iodo-2-deoxy-β-D-glucopyranose 

Downstream Products

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• 104206-20-4 1,6-anhydro-4-O-benzyl-2-chloro-2-deoxy-β-D-glucopyranose 
• 104206-19-1 1,6-anhydro-4-O-benzyl-2-deoxy-2-C-(2-propenyl)-β-D-glucopyranose 
• 110046-81-6 1,6-anhydro-4-O-benzyl-2-deoxy-2-C-(3-tert-butyldimethylsilyloxyprop-1-ynyl)-β-D-glucopyranose 
• 65190-43-4 4-O-benzyl-2-methyl-1,6-anhydro-β-D-glucopyranose 
• 129797-10-0 (1R,2S,3R,4R,5R)-2-Benzyloxy-4-trimethylsilanylethynyl-6,8-dioxa-bicyclo[3.2.1]octan-3-ol 
• 129797-08-6 (4aR,6S,7S,8S,8aS)-7-[3-(tert-Butyl-dimethyl-silanyloxy)-prop-1-ynyl]-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-ol 
• 89731-34-0 1,6-anhydro-4-O-benzyl-2-deoxy-2-C-(3-hydroxypropynyl)-β-D-glucopyranose 
• 117844-35-6 1,6-anhydro-4-O-benzyl-2-O-(prop-2-ynyl)-β-D-glucopyranose 
• 110046-91-8 1,6-anhydro-4-O-benzyl-2C-<3'-<(tert-butyldimethylsilyl)oxy>-2'-methylprop-1'(Z)-enyl>-β-D-glucopyranose 
• 110046-94-1 (1R,2S,3R,4R,5R)-2-Benzyloxy-4-((Z)-3-methoxymethoxy-2-methyl-propenyl)-6,8-dioxa-bicyclo[3.2.1]octan-3-ol 
• 40838-18-4 1,6-anhydro-4-O-benzyl-2,3-dideoxy-β-D-erythro-hex-2-enopyranose 
• 55682-47-8 1,6-anhydro-2-azido-4-O-benzyl-2-deoxy-β-D-glucopyranose 

Relevant articles and documents

AN EFFICIENT AND SCALABLE PROCESS FOR THE MANUFACTURE OF FONDAPARINUX SODIUM

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A facile synthesis of Cerny epoxides and selectively blocked derivatives of 2-azido-2-deoxy-β-D-glucopyranose

1,6:2,3-Dianhydro-β-D-glucopyranose and its 3-alkylated derivatives were prepared from D-glucal in one pot with overall isolated yields of 60-70%, and these Cerny epoxides were further conveniently converted to selectively blocked 2-azido-2-deoxy-β-D-glucopyranose derivatives by azido opening of the epoxide ring.