2-Methyl-2-(4-sulfamoylphenyl)propionic acid

95%

Reagent Code: #42180
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CAS Number 374067-95-5

science Other reagents with same CAS 374067-95-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.28 g/mol
Formula C₁₀H₁₃NO₄S
inventory_2 Storage & Handling
Density 1.353±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Primarily used as an intermediate in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs), this compound plays a crucial role in the development of medications aimed at reducing inflammation, pain, and fever. Its sulfamoyl group enhances its binding affinity to target enzymes, making it effective in inhibiting cyclooxygenase (COX) enzymes, which are responsible for producing prostaglandins that cause inflammation. Additionally, it is utilized in research settings to study the mechanisms of anti-inflammatory agents and to develop more efficient and safer therapeutic options. Its structural properties also make it a candidate for further chemical modifications to improve drug efficacy and reduce side effects.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿17,640.00
inventory 1g
10-20 days ฿64,260.00
inventory 100mg
10-20 days ฿11,970.00

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2-Methyl-2-(4-sulfamoylphenyl)propionic acid
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Primarily used as an intermediate in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs), this compound plays a crucial role in the development of medications aimed at reducing inflammation, pain, and fever. Its sulfamoyl group enhances its binding affinity to target enzymes, making it effective in inhibiting cyclooxygenase (COX) enzymes, which are responsible for producing prostaglandins that cause inflammation. Additionally, it is utilized in research settings to study the mechanisms of anti

Primarily used as an intermediate in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs), this compound plays a crucial role in the development of medications aimed at reducing inflammation, pain, and fever. Its sulfamoyl group enhances its binding affinity to target enzymes, making it effective in inhibiting cyclooxygenase (COX) enzymes, which are responsible for producing prostaglandins that cause inflammation. Additionally, it is utilized in research settings to study the mechanisms of anti-inflammatory agents and to develop more efficient and safer therapeutic options. Its structural properties also make it a candidate for further chemical modifications to improve drug efficacy and reduce side effects.

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