(S)-Methyl 2-(4-methylphenylsulfonamido)propanoate

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Reagent Code: #38148
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CAS Number 59724-69-5

science Other reagents with same CAS 59724-69-5

blur_circular Chemical Specifications

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Weight 257.3061 g/mol
Formula C₁₁H₁₅NO₄S
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key building block in the production of chiral molecules, which are essential for creating enantiomerically pure drugs. Its sulfonamide group and ester functionality make it a versatile reagent in organic synthesis, enabling the formation of complex structures with high specificity. Additionally, it is employed in research settings for studying enzyme inhibition and receptor binding activities, contributing to the discovery of new therapeutic agents. Its chiral nature also makes it valuable in asymmetric synthesis, where precise control over stereochemistry is required.

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inventory 100mg
10-20 days ฿2,313.00

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(S)-Methyl 2-(4-methylphenylsulfonamido)propanoate
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This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key building block in the production of chiral molecules, which are essential for creating enantiomerically pure drugs. Its sulfonamide group and ester functionality make it a versatile reagent in organic synthesis, enabling the formation of complex structures with high specificity. Additionally, it is employed in research settin

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key building block in the production of chiral molecules, which are essential for creating enantiomerically pure drugs. Its sulfonamide group and ester functionality make it a versatile reagent in organic synthesis, enabling the formation of complex structures with high specificity. Additionally, it is employed in research settings for studying enzyme inhibition and receptor binding activities, contributing to the discovery of new therapeutic agents. Its chiral nature also makes it valuable in asymmetric synthesis, where precise control over stereochemistry is required.

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