2-(1h-Imidazol-1-yl)benzenesulfonamide

98%

Reagent Code: #201150
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CAS Number 1094671-87-0

science Other reagents with same CAS 1094671-87-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.25 g/mol
Formula C₉H₉N₃O₂S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of bioactive compounds, particularly antifungal agents based on imidazole structures. The imidazole moiety inhibits cytochrome P450 enzymes in fungi, disrupting cell wall formation and preventing fungal growth, making it valuable in dermatological and systemic antifungal treatments.

Additionally, it is under investigation for antiviral drugs and central nervous system (CNS) therapeutics, as it can cross the blood-brain barrier to some degree, providing potential for designing brain-targeted medications.

In materials research, it acts as a ligand for transition metals, forming coordination complexes with special properties such as reaction acceleration or biomolecule detection.

It also shows promise in agrochemicals by improving the stability and efficacy of active ingredients in crop protection products.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,310.00
inventory 250mg
10-20 days ฿12,410.00
inventory 1g
10-20 days ฿33,470.00
2-(1h-Imidazol-1-yl)benzenesulfonamide
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Used as a key intermediate in the synthesis of bioactive compounds, particularly antifungal agents based on imidazole structures. The imidazole moiety inhibits cytochrome P450 enzymes in fungi, disrupting cell wall formation and preventing fungal growth, making it valuable in dermatological and systemic antifungal treatments.

Additionally, it is under investigation for antiviral drugs and central nervous system (CNS) therapeutics, as it can cross the blood-brain barrier to some degree, providing po

Used as a key intermediate in the synthesis of bioactive compounds, particularly antifungal agents based on imidazole structures. The imidazole moiety inhibits cytochrome P450 enzymes in fungi, disrupting cell wall formation and preventing fungal growth, making it valuable in dermatological and systemic antifungal treatments.

Additionally, it is under investigation for antiviral drugs and central nervous system (CNS) therapeutics, as it can cross the blood-brain barrier to some degree, providing potential for designing brain-targeted medications.

In materials research, it acts as a ligand for transition metals, forming coordination complexes with special properties such as reaction acceleration or biomolecule detection.

It also shows promise in agrochemicals by improving the stability and efficacy of active ingredients in crop protection products.

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