2-Formyl-N,N-dimethyl-1H-imidazole-1-sulfonamide

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Reagent Code: #43620
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CAS Number 167704-98-5

science Other reagents with same CAS 167704-98-5

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Weight 203.2190 g/mol
Formula C₆H₉N₃O₃S
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description Product Description

This chemical, featuring an imidazole core with a reactive formyl group at position 2 and an N,N-dimethylsulfonamide moiety at N1, is primarily utilized in organic synthesis as a versatile intermediate. It serves as a key building block in the development of pharmaceuticals, particularly in the creation of compounds with potential therapeutic properties. The formyl and sulfonamide groups enable diverse functionalization reactions, making it valuable in constructing complex molecular structures. Additionally, it is employed in the synthesis of heterocyclic compounds, which are often explored for their biological activities. Its role in medicinal chemistry research is significant, as it aids in the discovery and optimization of drug candidates.

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inventory 50mg
10-20 days ฿7,227.00

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2-Formyl-N,N-dimethyl-1H-imidazole-1-sulfonamide
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This chemical, featuring an imidazole core with a reactive formyl group at position 2 and an N,N-dimethylsulfonamide moiety at N1, is primarily utilized in organic synthesis as a versatile intermediate. It serves as a key building block in the development of pharmaceuticals, particularly in the creation of compounds with potential therapeutic properties. The formyl and sulfonamide groups enable diverse functionalization reactions, making it valuable in constructing complex molecular structures. Additiona

This chemical, featuring an imidazole core with a reactive formyl group at position 2 and an N,N-dimethylsulfonamide moiety at N1, is primarily utilized in organic synthesis as a versatile intermediate. It serves as a key building block in the development of pharmaceuticals, particularly in the creation of compounds with potential therapeutic properties. The formyl and sulfonamide groups enable diverse functionalization reactions, making it valuable in constructing complex molecular structures. Additionally, it is employed in the synthesis of heterocyclic compounds, which are often explored for their biological activities. Its role in medicinal chemistry research is significant, as it aids in the discovery and optimization of drug candidates.

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