(1S,2S)-1,2-Di((R)-1,4-dioxaspiro[4.5]decan-2-yl)ethane-1,2-diol

98%

Reagent Code: #84902
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CAS Number 76779-67-4

science Other reagents with same CAS 76779-67-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 342.43 g/mol
Formula C₁₈H₃₀O₆
thermostat Physical Properties
Melting Point 103-105 °C
inventory_2 Storage & Handling
Storage 2-8°C, inert atmosphere

description Product Description

This compound is primarily utilized in the field of organic synthesis as a chiral building block. Its unique structure, featuring spirocyclic dioxane units, makes it valuable for constructing complex molecules with high stereochemical control. It is often employed in the synthesis of pharmaceuticals, where precise chirality is crucial for biological activity. Additionally, it serves as a ligand or catalyst in asymmetric reactions, enhancing the efficiency and selectivity of processes such as hydrogenation or epoxidation. Its stability and ability to induce chirality make it a versatile tool in the development of enantiomerically pure compounds.

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Test Parameter Specification
APPEARANCE White Powder, Crystals, Crystalline Powder and/or Lumps
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿900.00
inventory 5g
10-20 days ฿4,050.00
inventory 1g
10-20 days ฿1,350.00

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(1S,2S)-1,2-Di((R)-1,4-dioxaspiro[4.5]decan-2-yl)ethane-1,2-diol
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This compound is primarily utilized in the field of organic synthesis as a chiral building block. Its unique structure, featuring spirocyclic dioxane units, makes it valuable for constructing complex molecules with high stereochemical control. It is often employed in the synthesis of pharmaceuticals, where precise chirality is crucial for biological activity. Additionally, it serves as a ligand or catalyst in asymmetric reactions, enhancing the efficiency and selectivity of processes such as hydrogenatio

This compound is primarily utilized in the field of organic synthesis as a chiral building block. Its unique structure, featuring spirocyclic dioxane units, makes it valuable for constructing complex molecules with high stereochemical control. It is often employed in the synthesis of pharmaceuticals, where precise chirality is crucial for biological activity. Additionally, it serves as a ligand or catalyst in asymmetric reactions, enhancing the efficiency and selectivity of processes such as hydrogenation or epoxidation. Its stability and ability to induce chirality make it a versatile tool in the development of enantiomerically pure compounds.

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