(2-(Difluoromethoxy)pyridin-4-yl)methanamine dihydrochloride

≥95%

Reagent Code: #129823
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CAS Number 2816370-66-6

science Other reagents with same CAS 2816370-66-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.07 g/mol
Formula C₇H₁₀Cl₂F₂N₂O
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure supports binding to specific enzyme active sites, enhancing selectivity and potency. Commonly employed in medicinal chemistry for constructing bioactive molecules due to the stability and polarity imparted by the difluoromethoxy and pyridine groups. Also utilized in the preparation of serotonin receptor modulators and antiviral compounds. The amine functionality allows for easy derivatization, making it valuable in library synthesis for drug discovery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,290.00
inventory 1g
10-20 days ฿6,000.00
inventory 5g
10-20 days ฿20,720.00

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(2-(Difluoromethoxy)pyridin-4-yl)methanamine dihydrochloride
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure supports binding to specific enzyme active sites, enhancing selectivity and potency. Commonly employed in medicinal chemistry for constructing bioactive molecules due to the stability and polarity imparted by the difluoromethoxy and pyridine groups. Also utilized in the preparation of serotonin receptor modulators and antiviral compounds.

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure supports binding to specific enzyme active sites, enhancing selectivity and potency. Commonly employed in medicinal chemistry for constructing bioactive molecules due to the stability and polarity imparted by the difluoromethoxy and pyridine groups. Also utilized in the preparation of serotonin receptor modulators and antiviral compounds. The amine functionality allows for easy derivatization, making it valuable in library synthesis for drug discovery.

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