β-D-Ribofuranose 1-acetate 2,3,5-tribenzoate

98%

Reagent Code: #58049
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Alias 1-Acetyl-2,3,5-tribenzoyloxy-1-beta-D-ribofuranose
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CAS Number 6974-32-9

science Other reagents with same CAS 6974-32-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 504.48 g/mol
Formula C₂₈H₂₄O₉
badge Registry Numbers
EC Number 230-220-4
MDL Number MFCD00005357
thermostat Physical Properties
Melting Point 128-130 °C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used in the synthesis of nucleosides and nucleotides, which are essential for creating antiviral and anticancer drugs. Acts as a protected intermediate in organic chemistry, enabling selective reactions without affecting other functional groups. Applied in carbohydrate chemistry for modifying sugar molecules to study biological processes or develop new pharmaceuticals. Also utilized in the preparation of glycosyl donors for oligosaccharide synthesis, aiding in the development of glycoconjugate vaccines and other therapeutic agents. Its benzoate groups provide stability during chemical transformations, making it valuable in complex organic synthesis.

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Test Parameter Specification
Heavy Metals (as Pb) 0-10 ppm
Melting point 127-130
Purity (GC) 98-100%
Specific Rotation (20°C, Pyridine) 23.9-24.9
Water (Karl Fischer) 0-1%
Appearance White powder or crystals
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿260.00
inventory 5g
10-20 days ฿290.00
inventory 25g
10-20 days ฿720.00
inventory 100g
10-20 days ฿2,180.00
inventory 500g
10-20 days ฿9,100.00

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β-D-Ribofuranose 1-acetate 2,3,5-tribenzoate
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Used in the synthesis of nucleosides and nucleotides, which are essential for creating antiviral and anticancer drugs. Acts as a protected intermediate in organic chemistry, enabling selective reactions without affecting other functional groups. Applied in carbohydrate chemistry for modifying sugar molecules to study biological processes or develop new pharmaceuticals. Also utilized in the preparation of glycosyl donors for oligosaccharide synthesis, aiding in the development of glycoconjugate vaccines a

Used in the synthesis of nucleosides and nucleotides, which are essential for creating antiviral and anticancer drugs. Acts as a protected intermediate in organic chemistry, enabling selective reactions without affecting other functional groups. Applied in carbohydrate chemistry for modifying sugar molecules to study biological processes or develop new pharmaceuticals. Also utilized in the preparation of glycosyl donors for oligosaccharide synthesis, aiding in the development of glycoconjugate vaccines and other therapeutic agents. Its benzoate groups provide stability during chemical transformations, making it valuable in complex organic synthesis.

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