3-(2-phenyl-1H-imidazol-1-yl)propanoic acid

≥95%

Reagent Code: #197963
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CAS Number 53660-14-3

science Other reagents with same CAS 53660-14-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.24 g/mol
Formula C₁₂H₁₂N₂O₂
badge Registry Numbers
MDL Number MFCD03043651
inventory_2 Storage & Handling
Storage 2-8°C, Sealed

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of histamine H3 receptor antagonists. It plays a role in developing compounds targeting neurological disorders such as Alzheimer's disease, attention deficit hyperactivity disorder (ADHD), and epilepsy due to its ability to modulate neurotransmitter release. The compound's structure allows for selective binding and improved metabolic stability in drug candidates. Also explored in the development of anti-inflammatory agents and in medicinal chemistry for optimizing lead compounds with enhanced bioavailability.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿21,420.00

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3-(2-phenyl-1H-imidazol-1-yl)propanoic acid
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Used in pharmaceutical research as a key intermediate in the synthesis of histamine H3 receptor antagonists. It plays a role in developing compounds targeting neurological disorders such as Alzheimer's disease, attention deficit hyperactivity disorder (ADHD), and epilepsy due to its ability to modulate neurotransmitter release. The compound's structure allows for selective binding and improved metabolic stability in drug candidates. Also explored in the development of anti-inflammatory agents and in medi

Used in pharmaceutical research as a key intermediate in the synthesis of histamine H3 receptor antagonists. It plays a role in developing compounds targeting neurological disorders such as Alzheimer's disease, attention deficit hyperactivity disorder (ADHD), and epilepsy due to its ability to modulate neurotransmitter release. The compound's structure allows for selective binding and improved metabolic stability in drug candidates. Also explored in the development of anti-inflammatory agents and in medicinal chemistry for optimizing lead compounds with enhanced bioavailability.

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