1,2,3,4,6-Penta-O-benzoyl-D-mannopyranose

≥98%

Reagent Code: #103610
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CAS Number 96996-90-6

science Other reagents with same CAS 96996-90-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 700.69 g/mol
Formula C₄₁H₃₂O₁₁
thermostat Physical Properties
Melting Point 152-153℃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used extensively in carbohydrate chemistry as a protected intermediate for synthesizing complex sugars and glycoconjugates. It serves as a key building block in the preparation of mannose derivatives, which are crucial for studying biological processes like cell signaling and immune response. Its benzoyl groups provide stability during chemical reactions, enabling precise modifications to the sugar backbone. This compound is also employed in the development of glycosylated pharmaceuticals, where specific sugar structures are required for drug efficacy. Additionally, it plays a role in creating synthetic oligosaccharides for research in glycobiology and vaccine development.

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Test Parameter Specification
Appearance White Powder
Purity (%) 97.5-100%
Infrared Spectrum Conforms To Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,050.00
inventory 25g
10-20 days ฿6,590.00
inventory 1g
10-20 days ฿891.00

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1,2,3,4,6-Penta-O-benzoyl-D-mannopyranose
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Used extensively in carbohydrate chemistry as a protected intermediate for synthesizing complex sugars and glycoconjugates. It serves as a key building block in the preparation of mannose derivatives, which are crucial for studying biological processes like cell signaling and immune response. Its benzoyl groups provide stability during chemical reactions, enabling precise modifications to the sugar backbone. This compound is also employed in the development of glycosylated pharmaceuticals, where specific

Used extensively in carbohydrate chemistry as a protected intermediate for synthesizing complex sugars and glycoconjugates. It serves as a key building block in the preparation of mannose derivatives, which are crucial for studying biological processes like cell signaling and immune response. Its benzoyl groups provide stability during chemical reactions, enabling precise modifications to the sugar backbone. This compound is also employed in the development of glycosylated pharmaceuticals, where specific sugar structures are required for drug efficacy. Additionally, it plays a role in creating synthetic oligosaccharides for research in glycobiology and vaccine development.

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