4-(N-(Butylcarbamoyl)sulfamoyl)benzoic acid

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Reagent Code: #47864
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CAS Number 2224-10-4

science Other reagents with same CAS 2224-10-4

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Weight 300.3308 g/mol
Formula C₁₂H₁₆N₂O₅S
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MDL Number MFCD00272697
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This chemical, 4-(N-(Butylcarbamoyl)sulfamoyl)benzoic acid, is primarily used as a key intermediate in the synthesis of sulfonylurea-based pharmaceuticals, particularly antidiabetic drugs for type 2 diabetes that stimulate insulin release from pancreatic beta cells and improve insulin sensitivity. It is also employed in the development of other sulfonamide derivatives with antimicrobial, diuretic, or enzyme-inhibiting properties. In research, it aids in studying biological interactions of sulfonamides. Additionally, its applications extend to agrochemical production, contributing to herbicides and pesticides. The compound's sulfonylurea-like structure enables effective interactions with biological targets in therapeutic and agricultural contexts.

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inventory 50mg
10-20 days ฿5,121.00

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4-(N-(Butylcarbamoyl)sulfamoyl)benzoic acid
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This chemical, 4-(N-(Butylcarbamoyl)sulfamoyl)benzoic acid, is primarily used as a key intermediate in the synthesis of sulfonylurea-based pharmaceuticals, particularly antidiabetic drugs for type 2 diabetes that stimulate insulin release from pancreatic beta cells and improve insulin sensitivity. It is also employed in the development of other sulfonamide derivatives with antimicrobial, diuretic, or enzyme-inhibiting properties. In research, it aids in studying biological interactions of sulfonamides. A

This chemical, 4-(N-(Butylcarbamoyl)sulfamoyl)benzoic acid, is primarily used as a key intermediate in the synthesis of sulfonylurea-based pharmaceuticals, particularly antidiabetic drugs for type 2 diabetes that stimulate insulin release from pancreatic beta cells and improve insulin sensitivity. It is also employed in the development of other sulfonamide derivatives with antimicrobial, diuretic, or enzyme-inhibiting properties. In research, it aids in studying biological interactions of sulfonamides. Additionally, its applications extend to agrochemical production, contributing to herbicides and pesticides. The compound's sulfonylurea-like structure enables effective interactions with biological targets in therapeutic and agricultural contexts.

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