2-(4-(2-(1H-Imidazol-1-yl)ethoxy)phenyl)ethanol

95%

Reagent Code: #197107
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CAS Number 99761-74-7

science Other reagents with same CAS 99761-74-7

blur_circular Chemical Specifications

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Weight 232.28 g/mol
Formula C₁₃H₁₆N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of histamine H3 receptor antagonists. Its structure supports the development of compounds targeting neurological disorders such as Alzheimer's disease, ADHD, and epilepsy. The presence of both imidazole and phenolic ether groups enables strong interactions with biological targets, enhancing receptor selectivity and binding affinity. Also explored in medicinal chemistry for optimizing drug candidates with improved metabolic stability and blood-brain barrier penetration.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,600.00
inventory 250mg
10-20 days ฿14,350.00
inventory 1g
10-20 days ฿41,970.00

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2-(4-(2-(1H-Imidazol-1-yl)ethoxy)phenyl)ethanol
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Used in pharmaceutical research as a key intermediate in the synthesis of histamine H3 receptor antagonists. Its structure supports the development of compounds targeting neurological disorders such as Alzheimer's disease, ADHD, and epilepsy. The presence of both imidazole and phenolic ether groups enables strong interactions with biological targets, enhancing receptor selectivity and binding affinity. Also explored in medicinal chemistry for optimizing drug candidates with improved metabolic stability a

Used in pharmaceutical research as a key intermediate in the synthesis of histamine H3 receptor antagonists. Its structure supports the development of compounds targeting neurological disorders such as Alzheimer's disease, ADHD, and epilepsy. The presence of both imidazole and phenolic ether groups enables strong interactions with biological targets, enhancing receptor selectivity and binding affinity. Also explored in medicinal chemistry for optimizing drug candidates with improved metabolic stability and blood-brain barrier penetration.

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