N-hydroxy-N-methyl-4-(2-methylpropyl)benzamide

95%

Reagent Code: #215314
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CAS Number 110319-76-1

science Other reagents with same CAS 110319-76-1

blur_circular Chemical Specifications

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Weight 207.27 g/mol
Formula C₁₂H₁₇NO₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceuticals. It serves as a key building block in the development of protease inhibitors and other enzyme-targeted therapeutics. Its hydroxamic acid functional group enables strong chelation with metal ions, making it valuable in the design of metalloenzyme inhibitors. Also employed in medicinal chemistry research for structure-activity relationship (SAR) studies due to its ability to mimic transition states in peptide hydrolysis. Additionally, it has been explored in the synthesis of anticancer and anti-inflammatory agents owing to its favorable binding properties with biological targets.

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inventory 250mg
10-20 days ฿20,000.00

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N-hydroxy-N-methyl-4-(2-methylpropyl)benzamide
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Used as an intermediate in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceuticals. It serves as a key building block in the development of protease inhibitors and other enzyme-targeted therapeutics. Its hydroxamic acid functional group enables strong chelation with metal ions, making it valuable in the design of metalloenzyme inhibitors. Also employed in medicinal chemistry research for structure-activity relationship (SAR) studies due to its ability to mimic transi

Used as an intermediate in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceuticals. It serves as a key building block in the development of protease inhibitors and other enzyme-targeted therapeutics. Its hydroxamic acid functional group enables strong chelation with metal ions, making it valuable in the design of metalloenzyme inhibitors. Also employed in medicinal chemistry research for structure-activity relationship (SAR) studies due to its ability to mimic transition states in peptide hydrolysis. Additionally, it has been explored in the synthesis of anticancer and anti-inflammatory agents owing to its favorable binding properties with biological targets.

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