CarbaMic acid, N-[(propylaMino)sulfonyl]-, phenylMethyl ester

98%

Reagent Code: #159479
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Alias Massititan intermediate
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CAS Number 92577-65-6

science Other reagents with same CAS 92577-65-6

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scatter_plot Molecular Information
Weight 272.32 g/mol
Formula C₁₁H₁₆N₂O₄S
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Used primarily as an intermediate in the synthesis of sulfonylurea herbicides. It plays a key role in agrochemical manufacturing due to its ability to form sulfamide linkages essential for herbicidal activity. The compound is also utilized in the development of certain pharmaceuticals where sulfonylurea moieties are required for biological activity. Its ester group allows for selective deprotection or transformation in multi-step organic syntheses. Commonly employed in research settings for designing new bioactive molecules with potential applications in crop protection and medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿1,490.00
inventory 1g
10-20 days ฿5,950.00
inventory 5g
10-20 days ฿8,860.50

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CarbaMic acid, N-[(propylaMino)sulfonyl]-, phenylMethyl ester
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Used primarily as an intermediate in the synthesis of sulfonylurea herbicides. It plays a key role in agrochemical manufacturing due to its ability to form sulfamide linkages essential for herbicidal activity. The compound is also utilized in the development of certain pharmaceuticals where sulfonylurea moieties are required for biological activity. Its ester group allows for selective deprotection or transformation in multi-step organic syntheses. Commonly employed in research settings for designing new

Used primarily as an intermediate in the synthesis of sulfonylurea herbicides. It plays a key role in agrochemical manufacturing due to its ability to form sulfamide linkages essential for herbicidal activity. The compound is also utilized in the development of certain pharmaceuticals where sulfonylurea moieties are required for biological activity. Its ester group allows for selective deprotection or transformation in multi-step organic syntheses. Commonly employed in research settings for designing new bioactive molecules with potential applications in crop protection and medicinal chemistry.

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