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

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Reagent Code: #217773
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CAS Number 193202-37-8

science Other reagents with same CAS 193202-37-8

blur_circular Chemical Specifications

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Weight 432.31 g/mol
Formula C₁₈H₁₉Cl₂NO₅S
badge Registry Numbers
MDL Number MFCD04117914
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 interaction with chiral amines and alcohols, making it valuable in asymmetric synthesis and stereochemical analysis. Commonly employed in high-performance liquid chromatography (HPLC) to form diastereomeric derivatives that can be easily separated and quantified. Also utilized in the development and purification of enantiomerically pure drugs, where precise stereochemistry is critical for biological activity.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,360.00
inventory 250mg
10-20 days ฿5,960.00
inventory 500mg
10-20 days ฿11,680.00

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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 interaction with chiral amines and alcohols, making it valuable in asymmetric synthesis and stereochemical analysis. Commonly employed in high-performance liquid chromatography (HPLC) to form diastereomeric derivatives that can be easily separated and quantified. Also utilized in the development and purification of enanti

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 interaction with chiral amines and alcohols, making it valuable in asymmetric synthesis and stereochemical analysis. Commonly employed in high-performance liquid chromatography (HPLC) to form diastereomeric derivatives that can be easily separated and quantified. Also utilized in the development and purification of enantiomerically pure drugs, where precise stereochemistry is critical for biological activity.

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