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

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Reagent Code: #37496
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CAS Number 511286-68-3

science Other reagents with same CAS 511286-68-3

blur_circular Chemical Specifications

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Weight 257.3061 g/mol
Formula C₁₁H₁₅NO₄S
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This chemical is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of chiral compounds. Its structure makes it a valuable intermediate in the production of enantiomerically pure drugs, which are crucial for ensuring the desired therapeutic effects and minimizing side effects. It is often employed in organic synthesis to create active pharmaceutical ingredients (APIs) for medications targeting conditions such as inflammation, pain, and microbial infections. Additionally, its sulfonamide group contributes to its role in creating compounds with potential antibacterial or antifungal properties. Researchers also use it in the study of stereochemistry and asymmetric synthesis to develop more efficient and selective chemical processes.

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inventory 100mg
10-20 days ฿1,242.00

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(R)-Methyl 2-(4-methylphenylsulfonamido)propanoate
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This chemical is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of chiral compounds. Its structure makes it a valuable intermediate in the production of enantiomerically pure drugs, which are crucial for ensuring the desired therapeutic effects and minimizing side effects. It is often employed in organic synthesis to create active pharmaceutical ingredients (APIs) for medications targeting conditions such as inflammation, pain, and microbial infections. Additional

This chemical is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of chiral compounds. Its structure makes it a valuable intermediate in the production of enantiomerically pure drugs, which are crucial for ensuring the desired therapeutic effects and minimizing side effects. It is often employed in organic synthesis to create active pharmaceutical ingredients (APIs) for medications targeting conditions such as inflammation, pain, and microbial infections. Additionally, its sulfonamide group contributes to its role in creating compounds with potential antibacterial or antifungal properties. Researchers also use it in the study of stereochemistry and asymmetric synthesis to develop more efficient and selective chemical processes.

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