3-(1H-Benzo[d]imidazol-2-yl)-N-methylpropan-1-amine

95%

Reagent Code: #196452
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CAS Number 64137-52-6

science Other reagents with same CAS 64137-52-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.26 g/mol
Formula C₁₁H₁₅N₃
badge Registry Numbers
MDL Number MFCD03163256
thermostat Physical Properties
Boiling Point 401 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, light-proof storage, inert atmosphere

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 central nervous system disorders such as narcolepsy, ADHD, and Alzheimer’s disease. Its structure supports binding affinity and selectivity for H3 receptors, making it valuable in optimizing drug candidates. Also explored in the development of anti-inflammatory and anticonvulsant agents due to its ability to modulate neurotransmitter release. Commonly utilized in medicinal chemistry for scaffold modification and structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,240.00
inventory 250mg
10-20 days ฿8,320.00
inventory 1g
10-20 days ฿16,640.00

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3-(1H-Benzo[d]imidazol-2-yl)-N-methylpropan-1-amine
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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 central nervous system disorders such as narcolepsy, ADHD, and Alzheimer’s disease. Its structure supports binding affinity and selectivity for H3 receptors, making it valuable in optimizing drug candidates. Also explored in the development of anti-inflammatory and anticonvulsant agents due to its ability to modulate neurotransmitter release. Commo

Used in pharmaceutical research as a key intermediate in the synthesis of histamine H3 receptor antagonists. It plays a role in developing compounds targeting central nervous system disorders such as narcolepsy, ADHD, and Alzheimer’s disease. Its structure supports binding affinity and selectivity for H3 receptors, making it valuable in optimizing drug candidates. Also explored in the development of anti-inflammatory and anticonvulsant agents due to its ability to modulate neurotransmitter release. Commonly utilized in medicinal chemistry for scaffold modification and structure-activity relationship (SAR) studies.

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