Methyl (1S)-()-10-Camphorsulfonate

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Reagent Code: #209923
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CAS Number 62319-13-5

science Other reagents with same CAS 62319-13-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.32 g/mol
Formula C₁₁H₁₈O₄S
thermostat Physical Properties
Melting Point 59 - 61 °C(lit.)
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral derivatizing agent in organic synthesis, particularly for the resolution of racemic mixtures. Its sulfonate group enables it to form esters with alcohols, allowing separation of enantiomers through crystallization or chromatography. Commonly employed in the preparation of optically pure intermediates for pharmaceuticals and fine chemicals. Also utilized in asymmetric synthesis due to its rigid camphor backbone, which imparts stereochemical control in reactions.

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Test Parameter Specification
Appearance white solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,250.00
inventory 250mg
10-20 days ฿3,650.00
inventory 1g
10-20 days ฿10,850.00
inventory 5g
10-20 days ฿37,500.00
inventory 25g
10-20 days ฿168,500.00

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Methyl (1S)-()-10-Camphorsulfonate
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Used as a chiral derivatizing agent in organic synthesis, particularly for the resolution of racemic mixtures. Its sulfonate group enables it to form esters with alcohols, allowing separation of enantiomers through crystallization or chromatography. Commonly employed in the preparation of optically pure intermediates for pharmaceuticals and fine chemicals. Also utilized in asymmetric synthesis due to its rigid camphor backbone, which imparts stereochemical control in reactions.

Used as a chiral derivatizing agent in organic synthesis, particularly for the resolution of racemic mixtures. Its sulfonate group enables it to form esters with alcohols, allowing separation of enantiomers through crystallization or chromatography. Commonly employed in the preparation of optically pure intermediates for pharmaceuticals and fine chemicals. Also utilized in asymmetric synthesis due to its rigid camphor backbone, which imparts stereochemical control in reactions.

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