(2R,3R,4S,5R)-2,3,4,5,6-Pentahydroxyhexanal

>95%

Reagent Code: #232236
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CAS Number 4205-23-6

science Other reagents with same CAS 4205-23-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.16 g/mol
Formula C₆H₁₂O₆
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MDL Number MFCD00069823
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

D-Idose, represented in its open-chain form as (2R,3R,4S,5R)-2,3,4,5,6-Pentahydroxyhexanal, is a rare aldohexose primarily used as a specialty reagent in biochemical and medicinal chemistry research. It functions as a key chiral building block in the synthesis of complex carbohydrates, including glycosides, oligosaccharides, and glycosaminoglycans such as heparin and dermatan sulfate via conversion to iduronic acid derivatives. Its distinctive stereochemistry and conformational flexibility make it valuable for studying carbohydrate structures, metabolic pathways, and asymmetric synthesis of enantiopure compounds in pharmaceutical development. Due to its scarcity and specialized applications, it is not commonly used in commercial food or cosmetic products.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿18,480.00
inventory 250mg
10-20 days ฿29,990.00

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(2R,3R,4S,5R)-2,3,4,5,6-Pentahydroxyhexanal
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D-Idose, represented in its open-chain form as (2R,3R,4S,5R)-2,3,4,5,6-Pentahydroxyhexanal, is a rare aldohexose primarily used as a specialty reagent in biochemical and medicinal chemistry research. It functions as a key chiral building block in the synthesis of complex carbohydrates, including glycosides, oligosaccharides, and glycosaminoglycans such as heparin and dermatan sulfate via conversion to iduronic acid derivatives. Its distinctive stereochemistry and conformational flexibility make it valuab

D-Idose, represented in its open-chain form as (2R,3R,4S,5R)-2,3,4,5,6-Pentahydroxyhexanal, is a rare aldohexose primarily used as a specialty reagent in biochemical and medicinal chemistry research. It functions as a key chiral building block in the synthesis of complex carbohydrates, including glycosides, oligosaccharides, and glycosaminoglycans such as heparin and dermatan sulfate via conversion to iduronic acid derivatives. Its distinctive stereochemistry and conformational flexibility make it valuable for studying carbohydrate structures, metabolic pathways, and asymmetric synthesis of enantiopure compounds in pharmaceutical development. Due to its scarcity and specialized applications, it is not commonly used in commercial food or cosmetic products.

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