2,3,4,6-Tetra-O-pivaloyl-β-D-galactopyranosylamine

99%

Reagent Code: #98137
label
Alias Tetra-O-pivaloyl-β-D-galactosamine
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CAS Number 108342-87-6

science Other reagents with same CAS 108342-87-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 515.64 g/mol
Formula C₂₆H₄₅NO₉
badge Registry Numbers
MDL Number MFCD00153054
thermostat Physical Properties
Melting Point 92-95 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used primarily in organic synthesis as a protected form of galactosamine, this compound serves as a key intermediate in the production of complex carbohydrates and glycoconjugates. Its pivaloyl groups provide stability during chemical reactions, making it suitable for glycosylation processes. It is also employed in the development of glycosidase inhibitors and in the study of carbohydrate-protein interactions. Additionally, it finds application in the synthesis of bioactive molecules, including potential drug candidates for treating bacterial infections and cancer. Its role in glycobiology research is significant, aiding in the exploration of cell signaling and immune response mechanisms.

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Test Parameter Specification
Melting Point 92-95
Purity 99-100%
Appearance White to light yellow powder
Infrared Spectrometry Conforms to Structure

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inventory 1g
10-20 days ฿10,570.00

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2,3,4,6-Tetra-O-pivaloyl-β-D-galactopyranosylamine
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Used primarily in organic synthesis as a protected form of galactosamine, this compound serves as a key intermediate in the production of complex carbohydrates and glycoconjugates. Its pivaloyl groups provide stability during chemical reactions, making it suitable for glycosylation processes. It is also employed in the development of glycosidase inhibitors and in the study of carbohydrate-protein interactions. Additionally, it finds application in the synthesis of bioactive molecules, including potential

Used primarily in organic synthesis as a protected form of galactosamine, this compound serves as a key intermediate in the production of complex carbohydrates and glycoconjugates. Its pivaloyl groups provide stability during chemical reactions, making it suitable for glycosylation processes. It is also employed in the development of glycosidase inhibitors and in the study of carbohydrate-protein interactions. Additionally, it finds application in the synthesis of bioactive molecules, including potential drug candidates for treating bacterial infections and cancer. Its role in glycobiology research is significant, aiding in the exploration of cell signaling and immune response mechanisms.

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