(2-Phenyl-1H-imidazol-4-yl)methanol

98%

Reagent Code: #227595
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CAS Number 43002-54-6

science Other reagents with same CAS 43002-54-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.2 g/mol
Formula C₁₀H₁₀N₂O
badge Registry Numbers
MDL Number MFCD06202903
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals, particularly in the development of histamine H3 receptor antagonists and antifungal agents. Serves as a building block in the preparation of imidazole-based bioactive molecules due to its reactive hydroxymethyl group. Also employed in medicinal chemistry for structure-activity relationship studies targeting central nervous system disorders. Its polar functionality aids in improving solubility and binding affinity in drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,180.00
inventory 250mg
10-20 days ฿1,760.00
inventory 1g
10-20 days ฿4,640.00
inventory 5g
10-20 days ฿16,100.00
inventory 10g
10-20 days ฿30,660.00

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(2-Phenyl-1H-imidazol-4-yl)methanol
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Used in organic synthesis as an intermediate for pharmaceuticals, particularly in the development of histamine H3 receptor antagonists and antifungal agents. Serves as a building block in the preparation of imidazole-based bioactive molecules due to its reactive hydroxymethyl group. Also employed in medicinal chemistry for structure-activity relationship studies targeting central nervous system disorders. Its polar functionality aids in improving solubility and binding affinity in drug candidates.

Used in organic synthesis as an intermediate for pharmaceuticals, particularly in the development of histamine H3 receptor antagonists and antifungal agents. Serves as a building block in the preparation of imidazole-based bioactive molecules due to its reactive hydroxymethyl group. Also employed in medicinal chemistry for structure-activity relationship studies targeting central nervous system disorders. Its polar functionality aids in improving solubility and binding affinity in drug candidates.

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