Methyl 2-(N-(tert-butoxycarbonyl)-4-MethylphenylsulfonaMido)acrylate

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Reagent Code: #59558
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CAS Number 219851-87-3

science Other reagents with same CAS 219851-87-3

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Weight 355.41 g/mol
Formula C₁₆H₂₁NO₆S
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in the development of complex molecules. It serves as a key intermediate in the production of pharmaceuticals, where its structure is valuable for constructing specific functional groups. The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for safeguarding amines during multi-step synthetic processes, allowing selective reactions to occur without interference. Additionally, the sulfonamide moiety enhances its application in designing compounds with potential biological activity, such as enzyme inhibitors or receptor modulators. Its acrylate functionality further enables participation in polymerization reactions, making it useful in material science for creating specialized polymers. Overall, this compound plays a significant role in advancing research and development in medicinal chemistry and polymer science.

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inventory 1g
10-20 days ฿8,775.00

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Methyl 2-(N-(tert-butoxycarbonyl)-4-MethylphenylsulfonaMido)acrylate
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This chemical is primarily utilized in organic synthesis, particularly in the development of complex molecules. It serves as a key intermediate in the production of pharmaceuticals, where its structure is valuable for constructing specific functional groups. The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for safeguarding amines during multi-step synthetic processes, allowing selective reactions to occur without interference. Additionally, the sulfonamide moiety enhances its app

This chemical is primarily utilized in organic synthesis, particularly in the development of complex molecules. It serves as a key intermediate in the production of pharmaceuticals, where its structure is valuable for constructing specific functional groups. The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for safeguarding amines during multi-step synthetic processes, allowing selective reactions to occur without interference. Additionally, the sulfonamide moiety enhances its application in designing compounds with potential biological activity, such as enzyme inhibitors or receptor modulators. Its acrylate functionality further enables participation in polymerization reactions, making it useful in material science for creating specialized polymers. Overall, this compound plays a significant role in advancing research and development in medicinal chemistry and polymer science.

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