4-Bromo-2-(1H-imidazol-2-yl)phenol

95%

Reagent Code: #47350
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CAS Number 289506-17-8

science Other reagents with same CAS 289506-17-8

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Weight 239.0687 g/mol
Formula C₉H₇BrN₂O
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MDL Number MFCD08668760
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This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceutical compounds. Its structure, featuring both an imidazole ring and a phenol group, makes it valuable for developing molecules with potential biological activity. It is often employed in the synthesis of antifungal and antibacterial agents, leveraging the imidazole moiety’s ability to interact with microbial enzymes. Additionally, its bromine substituent allows for further functionalization through cross-coupling reactions, enabling the creation of more complex chemical entities. Researchers also explore its use in designing ligands for metal coordination, which can be applied in catalysis or material science. Its versatility makes it a useful building block in medicinal chemistry and drug discovery efforts.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,379.00

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4-Bromo-2-(1H-imidazol-2-yl)phenol
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This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceutical compounds. Its structure, featuring both an imidazole ring and a phenol group, makes it valuable for developing molecules with potential biological activity. It is often employed in the synthesis of antifungal and antibacterial agents, leveraging the imidazole moiety’s ability to interact with microbial enzymes. Additionally, its bromine substituent allo

This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceutical compounds. Its structure, featuring both an imidazole ring and a phenol group, makes it valuable for developing molecules with potential biological activity. It is often employed in the synthesis of antifungal and antibacterial agents, leveraging the imidazole moiety’s ability to interact with microbial enzymes. Additionally, its bromine substituent allows for further functionalization through cross-coupling reactions, enabling the creation of more complex chemical entities. Researchers also explore its use in designing ligands for metal coordination, which can be applied in catalysis or material science. Its versatility makes it a useful building block in medicinal chemistry and drug discovery efforts.

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