(1R,2S,3S,4R)-CYCLOHEX-5-ENE-1,2,3,4-TETRAOL

97%

Reagent Code: #232350
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CAS Number 25348-64-5

science Other reagents with same CAS 25348-64-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 146.14 g/mol
Formula C₆H₁₀O₄
badge Registry Numbers
MDL Number MFCD00269953
thermostat Physical Properties
Melting Point 201-203 °C
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a chiral building block in organic synthesis, particularly in the development of pharmaceuticals and biologically active compounds. Its rigid cyclohexene backbone and multiple hydroxyl groups in defined stereochemistry make it valuable for constructing complex molecules with high stereoselectivity. Commonly employed in the synthesis of antiviral and antitumor agents, where precise spatial arrangement of functional groups is critical. Also explored in the preparation of carbohydrate mimetics and enzyme inhibitors due to its structural similarity to sugar moieties. Its hydrophilic nature and functional handles allow for further derivatization in medicinal chemistry and drug design.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿20,290.00
inventory 250mg
10-20 days ฿33,820.00
inventory 1g
10-20 days ฿82,430.00
(1R,2S,3S,4R)-CYCLOHEX-5-ENE-1,2,3,4-TETRAOL
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Used as a chiral building block in organic synthesis, particularly in the development of pharmaceuticals and biologically active compounds. Its rigid cyclohexene backbone and multiple hydroxyl groups in defined stereochemistry make it valuable for constructing complex molecules with high stereoselectivity. Commonly employed in the synthesis of antiviral and antitumor agents, where precise spatial arrangement of functional groups is critical. Also explored in the preparation of carbohydrate mimetics and e

Used as a chiral building block in organic synthesis, particularly in the development of pharmaceuticals and biologically active compounds. Its rigid cyclohexene backbone and multiple hydroxyl groups in defined stereochemistry make it valuable for constructing complex molecules with high stereoselectivity. Commonly employed in the synthesis of antiviral and antitumor agents, where precise spatial arrangement of functional groups is critical. Also explored in the preparation of carbohydrate mimetics and enzyme inhibitors due to its structural similarity to sugar moieties. Its hydrophilic nature and functional handles allow for further derivatization in medicinal chemistry and drug design.

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