(1H-Imidazol-1-yl)(phenyl)methanone
95%
- Product Code: 36186
CAS:
10364-94-0
Molecular Weight: | 172.1833 g./mol | Molecular Formula: | C₁₀H₈N₂O |
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EC Number: | MDL Number: | MFCD00014499 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
(1H-Imidazol-1-yl)(phenyl)methanone is primarily used in organic synthesis as a versatile intermediate for the preparation of various biologically active compounds. Its structure, featuring both an imidazole ring and a phenyl group, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of antifungal and antimicrobial agents. The imidazole moiety is known for its role in inhibiting enzymes like cytochrome P450, which is crucial in drug metabolism, making this compound useful in designing enzyme inhibitors. Additionally, it serves as a building block in the creation of heterocyclic compounds, which are widely explored for their potential in medicinal chemistry and agrochemical applications. Its reactivity also allows for modifications to produce derivatives with tailored properties for specific industrial or research purposes.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿846.00 |
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(1H-Imidazol-1-yl)(phenyl)methanone
(1H-Imidazol-1-yl)(phenyl)methanone is primarily used in organic synthesis as a versatile intermediate for the preparation of various biologically active compounds. Its structure, featuring both an imidazole ring and a phenyl group, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of antifungal and antimicrobial agents. The imidazole moiety is known for its role in inhibiting enzymes like cytochrome P450, which is crucial in drug metabolism, making this compound useful in designing enzyme inhibitors. Additionally, it serves as a building block in the creation of heterocyclic compounds, which are widely explored for their potential in medicinal chemistry and agrochemical applications. Its reactivity also allows for modifications to produce derivatives with tailored properties for specific industrial or research purposes.
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