[4-(1H-1,3-benzimidazol-1-yl)phenyl]methanol

95%

Reagent Code: #196373
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CAS Number 451485-67-9

science Other reagents with same CAS 451485-67-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.26 g/mol
Formula C₁₄H₁₂N₂O
badge Registry Numbers
MDL Number MFCD03425763
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used in pharmaceutical research as an intermediate for synthesizing bioactive molecules, particularly in the development of antiparasitic and antiviral agents. Its structure supports binding to biological targets due to the benzimidazole core, which is known for interacting with enzymes and receptors in pathogenic organisms. Also explored in the design of fluorescent probes for cellular imaging owing to its favorable photophysical properties. Commonly employed in medicinal chemistry for modifying drug candidates to improve solubility and bioavailability.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿3,560.00
100mg
10-20 days ฿9,060.00
[4-(1H-1,3-benzimidazol-1-yl)phenyl]methanol
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Used in pharmaceutical research as an intermediate for synthesizing bioactive molecules, particularly in the development of antiparasitic and antiviral agents. Its structure supports binding to biological targets due to the benzimidazole core, which is known for interacting with enzymes and receptors in pathogenic organisms. Also explored in the design of fluorescent probes for cellular imaging owing to its favorable photophysical properties. Commonly employed in medicinal chemistry for modifying drug candi
Used in pharmaceutical research as an intermediate for synthesizing bioactive molecules, particularly in the development of antiparasitic and antiviral agents. Its structure supports binding to biological targets due to the benzimidazole core, which is known for interacting with enzymes and receptors in pathogenic organisms. Also explored in the design of fluorescent probes for cellular imaging owing to its favorable photophysical properties. Commonly employed in medicinal chemistry for modifying drug candidates to improve solubility and bioavailability.
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