4-Methyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine dihydrochloride

95%

Reagent Code: #203322
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CAS Number 62002-35-1

science Other reagents with same CAS 62002-35-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.1 g/mol
Formula C₇H₁₃Cl₂N₃
badge Registry Numbers
MDL Number MFCD28894314
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of histamine H3 receptor antagonists. It plays a key role in creating compounds for neurological disorders such as narcolepsy, ADHD, and cognitive impairments. Its structure supports binding to central nervous system targets, making it valuable in medicinal chemistry for drug design. Also utilized in research settings to explore receptor selectivity and improve blood-brain barrier penetration in neuroactive agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,160.00
inventory 250mg
10-20 days ฿15,570.00

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4-Methyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine dihydrochloride
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of histamine H3 receptor antagonists. It plays a key role in creating compounds for neurological disorders such as narcolepsy, ADHD, and cognitive impairments. Its structure supports binding to central nervous system targets, making it valuable in medicinal chemistry for drug design. Also utilized in research settings to explore receptor selectivity and improve blood-brain barrier penetration in neuroactive agent

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of histamine H3 receptor antagonists. It plays a key role in creating compounds for neurological disorders such as narcolepsy, ADHD, and cognitive impairments. Its structure supports binding to central nervous system targets, making it valuable in medicinal chemistry for drug design. Also utilized in research settings to explore receptor selectivity and improve blood-brain barrier penetration in neuroactive agents.

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