4-Methoxyphenyl 4,6-O-Benzylidene-β-D-galactopyranoside

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Reagent Code: #103739
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CAS Number 176299-96-0

science Other reagents with same CAS 176299-96-0

blur_circular Chemical Specifications

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Weight 374.39 g/mol
Formula C₂₀H₂₂O₇
inventory_2 Storage & Handling
Storage -20℃

description Product Description

This compound is primarily utilized in carbohydrate chemistry research, particularly in the synthesis and study of complex sugars and glycoconjugates. It serves as a key intermediate in the preparation of glycosides, which are important for understanding biological processes such as cell signaling and recognition. Additionally, it is used in the development of glycodendrimers and other carbohydrate-based materials for potential applications in drug delivery systems and biomedical devices. Its benzylidene protecting group allows for selective modifications, making it valuable in the design of novel glycosylation strategies.

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inventory 1mg
10-20 days ฿9,500.00

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4-Methoxyphenyl 4,6-O-Benzylidene-β-D-galactopyranoside
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This compound is primarily utilized in carbohydrate chemistry research, particularly in the synthesis and study of complex sugars and glycoconjugates. It serves as a key intermediate in the preparation of glycosides, which are important for understanding biological processes such as cell signaling and recognition. Additionally, it is used in the development of glycodendrimers and other carbohydrate-based materials for potential applications in drug delivery systems and biomedical devices. Its benzylidene

This compound is primarily utilized in carbohydrate chemistry research, particularly in the synthesis and study of complex sugars and glycoconjugates. It serves as a key intermediate in the preparation of glycosides, which are important for understanding biological processes such as cell signaling and recognition. Additionally, it is used in the development of glycodendrimers and other carbohydrate-based materials for potential applications in drug delivery systems and biomedical devices. Its benzylidene protecting group allows for selective modifications, making it valuable in the design of novel glycosylation strategies.

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