(4S)-Methyl-[1,3,2]dioxathiolane 2,2-dioxide

95%

Reagent Code: #36982
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CAS Number 174953-30-1

science Other reagents with same CAS 174953-30-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 138.1423 g/mol
Formula C₃H₆O₄S
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MDL Number MFCD26131320
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description Product Description

This compound is primarily used in the field of organic synthesis as a versatile building block for creating more complex molecules. It is particularly valuable in the development of chiral compounds due to its stereospecific structure, which allows for the introduction of asymmetry in synthetic pathways. It is also employed in the preparation of sulfonates and sulfates, which are crucial intermediates in pharmaceuticals and agrochemicals. Additionally, its unique dioxathiolane ring structure makes it useful in polymer chemistry for modifying the properties of materials, such as enhancing thermal stability or introducing specific functional groups.

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Test Parameter Specification
Appearance Colorless to Light Yellow to Light Brown Liquid
Purity (%) 94.5-100%
Specific Rotation ([a]20/D, C=1g/100ml, CHCl3) (°) 25-32
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,158.00

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(4S)-Methyl-[1,3,2]dioxathiolane 2,2-dioxide
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This compound is primarily used in the field of organic synthesis as a versatile building block for creating more complex molecules. It is particularly valuable in the development of chiral compounds due to its stereospecific structure, which allows for the introduction of asymmetry in synthetic pathways. It is also employed in the preparation of sulfonates and sulfates, which are crucial intermediates in pharmaceuticals and agrochemicals. Additionally, its unique dioxathiolane ring structure makes it us

This compound is primarily used in the field of organic synthesis as a versatile building block for creating more complex molecules. It is particularly valuable in the development of chiral compounds due to its stereospecific structure, which allows for the introduction of asymmetry in synthetic pathways. It is also employed in the preparation of sulfonates and sulfates, which are crucial intermediates in pharmaceuticals and agrochemicals. Additionally, its unique dioxathiolane ring structure makes it useful in polymer chemistry for modifying the properties of materials, such as enhancing thermal stability or introducing specific functional groups.

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