N-(2-Carboxy-4,5-dichlorobenzoyl)-()-10,2-camphorsultam

≥98.0%(T)(HPLC)

Reagent Code: #215113
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CAS Number 1820575-29-8

science Other reagents with same CAS 1820575-29-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 432.31 g/mol
Formula C₁₈H₁₉Cl₂NO₅S
badge Registry Numbers
MDL Number MFCD04117916
thermostat Physical Properties
Melting Point 208 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral derivatizing agent in the resolution of racemic mixtures, particularly for the separation of enantiomers in pharmaceutical compounds. Its structure allows for selective binding to specific enantiomeric forms, making it valuable in high-performance liquid chromatography (HPLC) and capillary electrophoresis. It is also employed in asymmetric synthesis to control stereochemistry in complex organic molecules, especially in the development of active pharmaceutical ingredients where chirality affects biological activity.

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inventory 250g
10-20 days ฿5,550.00

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N-(2-Carboxy-4,5-dichlorobenzoyl)-()-10,2-camphorsultam
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Used as a chiral derivatizing agent in the resolution of racemic mixtures, particularly for the separation of enantiomers in pharmaceutical compounds. Its structure allows for selective binding to specific enantiomeric forms, making it valuable in high-performance liquid chromatography (HPLC) and capillary electrophoresis. It is also employed in asymmetric synthesis to control stereochemistry in complex organic molecules, especially in the development of active pharmaceutical ingredients where chirality

Used as a chiral derivatizing agent in the resolution of racemic mixtures, particularly for the separation of enantiomers in pharmaceutical compounds. Its structure allows for selective binding to specific enantiomeric forms, making it valuable in high-performance liquid chromatography (HPLC) and capillary electrophoresis. It is also employed in asymmetric synthesis to control stereochemistry in complex organic molecules, especially in the development of active pharmaceutical ingredients where chirality affects biological activity.

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