Methyl 4,6-O-Benzylidene-2-deoxy-α-D-erythro-hexopyranosid-3-ulose Oxime

≥98%(HPLC)(T)

Reagent Code: #82755
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CAS Number 63598-32-3

science Other reagents with same CAS 63598-32-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.29 g/mol
Formula C₁₄H₁₇NO₅
thermostat Physical Properties
Melting Point 200°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly in the development of complex carbohydrate derivatives. It serves as a key intermediate in the preparation of various biologically active compounds, including glycosidase inhibitors and other carbohydrate-based pharmaceuticals. Its unique structure allows for selective modifications, enabling researchers to explore and design novel therapeutic agents targeting specific enzymes or receptors. Additionally, it is employed in the study of carbohydrate chemistry to understand reaction mechanisms and stereochemical outcomes, aiding in the advancement of synthetic methodologies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,533.00

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Methyl 4,6-O-Benzylidene-2-deoxy-α-D-erythro-hexopyranosid-3-ulose Oxime
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This chemical is primarily utilized in the field of organic synthesis, particularly in the development of complex carbohydrate derivatives. It serves as a key intermediate in the preparation of various biologically active compounds, including glycosidase inhibitors and other carbohydrate-based pharmaceuticals. Its unique structure allows for selective modifications, enabling researchers to explore and design novel therapeutic agents targeting specific enzymes or receptors. Additionally, it is employed in th
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of complex carbohydrate derivatives. It serves as a key intermediate in the preparation of various biologically active compounds, including glycosidase inhibitors and other carbohydrate-based pharmaceuticals. Its unique structure allows for selective modifications, enabling researchers to explore and design novel therapeutic agents targeting specific enzymes or receptors. Additionally, it is employed in the study of carbohydrate chemistry to understand reaction mechanisms and stereochemical outcomes, aiding in the advancement of synthetic methodologies.
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