6-(4-Methoxyphenoxy)pyridazin-3-amine

95%

Reagent Code: #206867
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CAS Number 121041-41-6

science Other reagents with same CAS 121041-41-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.22 g/mol
Formula C₁₁H₁₁N₃O₂
badge Registry Numbers
MDL Number MFCD09839352
thermostat Physical Properties
Boiling Point 443.8°C
inventory_2 Storage & Handling
Storage 2-8°C

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. Also employed in agrochemical research for designing novel herbicides due to its ability to interfere with plant growth regulation. The compound's stability and reactivity profile make it suitable for further functionalization in medicinal chemistry campaigns.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿930.00
inventory 250mg
10-20 days ฿2,200.00

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6-(4-Methoxyphenoxy)pyridazin-3-amine
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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. Also employed in agrochemical research for designing novel herbicides due to its ability to interfere with plant growth regulation. The compound's stability and reactivity profile make it suitable for further functionalization in medicinal chemistry campai

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. Also employed in agrochemical research for designing novel herbicides due to its ability to interfere with plant growth regulation. The compound's stability and reactivity profile make it suitable for further functionalization in medicinal chemistry campaigns.

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