3-Chloro-5-methoxypyridin-4-amine

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Reagent Code: #132167
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CAS Number 1261471-70-8

science Other reagents with same CAS 1261471-70-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.59 g/mol
Formula C₆H₇ClN₂O
badge Registry Numbers
MDL Number MFCD18415425
thermostat Physical Properties
Boiling Point 278.5±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.311±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of active pharmaceutical ingredients (APIs) due to its reactive amine and halogen groups, which allow for further functionalization. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in optimizing pyridine-based drug candidates. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿7,880.00
inventory 100mg
10-20 days ฿12,610.00
inventory 250mg
10-20 days ฿23,210.00

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3-Chloro-5-methoxypyridin-4-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of active pharmaceutical ingredients (APIs) due to its reactive amine and halogen groups, which allow for further functionalization. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in optimizing pyridine-based drug candidates. Also utilized in agrochemical research

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of active pharmaceutical ingredients (APIs) due to its reactive amine and halogen groups, which allow for further functionalization. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in optimizing pyridine-based drug candidates. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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