6-Methoxy-N2-methylpyridine-2,3-diamine Dihydrochloride Hydrate

98%, dark blue purple crystalline powder

Reagent Code: #209528
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CAS Number 83732-72-3

science Other reagents with same CAS 83732-72-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.10(anhy) g/mol
Formula C₇H₁₃Cl₂N₃O(anhy)
badge Registry Numbers
MDL Number MFCD08543464
thermostat Physical Properties
Boiling Point 313.5 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used in pharmaceutical synthesis as an intermediate for developing kinase inhibitors, particularly in the production of selective inhibitors targeting cancer-related enzymes. Commonly employed in research for antitumor drug development due to its ability to enhance binding selectivity in molecular structures. Also utilized in the preparation of bioactive compounds for neurological disorder studies, where its methoxy and amine functionalities contribute to blood-brain barrier penetration. Frequently applied in medicinal chemistry for structure-activity relationship (SAR) studies involving pyridine-based scaffolds.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,470.00
inventory 5g
10-20 days ฿15,560.00

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6-Methoxy-N2-methylpyridine-2,3-diamine Dihydrochloride Hydrate
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Used in pharmaceutical synthesis as an intermediate for developing kinase inhibitors, particularly in the production of selective inhibitors targeting cancer-related enzymes. Commonly employed in research for antitumor drug development due to its ability to enhance binding selectivity in molecular structures. Also utilized in the preparation of bioactive compounds for neurological disorder studies, where its methoxy and amine functionalities contribute to blood-brain barrier penetration. Frequently appli

Used in pharmaceutical synthesis as an intermediate for developing kinase inhibitors, particularly in the production of selective inhibitors targeting cancer-related enzymes. Commonly employed in research for antitumor drug development due to its ability to enhance binding selectivity in molecular structures. Also utilized in the preparation of bioactive compounds for neurological disorder studies, where its methoxy and amine functionalities contribute to blood-brain barrier penetration. Frequently applied in medicinal chemistry for structure-activity relationship (SAR) studies involving pyridine-based scaffolds.

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