(R)-1-(4-Phenyl-1H-imidazol-2-yl)ethanamine

95%

Reagent Code: #229261
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CAS Number 335246-81-6

science Other reagents with same CAS 335246-81-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.24 g/mol
Formula C₁₁H₁₃N₃
badge Registry Numbers
MDL Number MFCD20668749
thermostat Physical Properties
Boiling Point 422.1±28.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.145±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of histamine H3 receptor antagonists. It serves as a chiral building block in drug discovery for neurological disorders such as narcolepsy, ADHD, and Alzheimer's disease. Its structural features enable selective binding to receptors in the central nervous system, making it valuable in creating compounds with improved efficacy and reduced side effects. Also employed in asymmetric synthesis due to its chiral amine functionality, supporting the production of enantiomerically pure drugs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,570.00
inventory 250mg
10-20 days ฿7,750.00
inventory 1g
10-20 days ฿20,300.00

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(R)-1-(4-Phenyl-1H-imidazol-2-yl)ethanamine
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of histamine H3 receptor antagonists. It serves as a chiral building block in drug discovery for neurological disorders such as narcolepsy, ADHD, and Alzheimer's disease. Its structural features enable selective binding to receptors in the central nervous system, making it valuable in creating compounds with improved efficacy and reduced side effects. Also employed in asymmetric synthesis due to its chiral amine functi

Used in the synthesis of pharmaceutical intermediates, particularly in the development of histamine H3 receptor antagonists. It serves as a chiral building block in drug discovery for neurological disorders such as narcolepsy, ADHD, and Alzheimer's disease. Its structural features enable selective binding to receptors in the central nervous system, making it valuable in creating compounds with improved efficacy and reduced side effects. Also employed in asymmetric synthesis due to its chiral amine functionality, supporting the production of enantiomerically pure drugs.

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