Ethyl 3-O-Benzyl-4,6-O-benzylidene-2-phthalimido-2-deoxy-1-thio-β-D-glucopyranoside

≥98%

Reagent Code: #103883
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CAS Number 129519-27-3

science Other reagents with same CAS 129519-27-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 531.6 g/mol
Formula C₃₀H₂₉NO₆S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis and carbohydrate chemistry as a key intermediate for the preparation of complex glycoconjugates and glycosides. Its structure, featuring protective benzyl and benzylidene groups, makes it valuable for selective deprotection strategies, enabling the synthesis of specific glycosidic linkages. The phthalimido group serves as a protective moiety for amino functionalities, which is crucial in the synthesis of amino sugars. Additionally, the thio-glycoside linkage enhances its stability and reactivity, making it suitable for glycosylation reactions in the development of bioactive molecules, such as glycopeptides, glycolipids, and other glycosylated natural products. Its application extends to the study of enzymatic glycosylation processes and the design of carbohydrate-based drugs.

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Test Parameter Specification
Appearance White to off-white powder
Purity (%) 97.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿2,450.00
inventory 25mg
10-20 days ฿9,240.00

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Ethyl 3-O-Benzyl-4,6-O-benzylidene-2-phthalimido-2-deoxy-1-thio-β-D-glucopyranoside
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This compound is primarily utilized in organic synthesis and carbohydrate chemistry as a key intermediate for the preparation of complex glycoconjugates and glycosides. Its structure, featuring protective benzyl and benzylidene groups, makes it valuable for selective deprotection strategies, enabling the synthesis of specific glycosidic linkages. The phthalimido group serves as a protective moiety for amino functionalities, which is crucial in the synthesis of amino sugars. Additionally, the thio-glycosi

This compound is primarily utilized in organic synthesis and carbohydrate chemistry as a key intermediate for the preparation of complex glycoconjugates and glycosides. Its structure, featuring protective benzyl and benzylidene groups, makes it valuable for selective deprotection strategies, enabling the synthesis of specific glycosidic linkages. The phthalimido group serves as a protective moiety for amino functionalities, which is crucial in the synthesis of amino sugars. Additionally, the thio-glycoside linkage enhances its stability and reactivity, making it suitable for glycosylation reactions in the development of bioactive molecules, such as glycopeptides, glycolipids, and other glycosylated natural products. Its application extends to the study of enzymatic glycosylation processes and the design of carbohydrate-based drugs.

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