5-Chloro-2-methyl-pyridin-3-ylamine

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Reagent Code: #163605
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CAS Number 89639-36-1

science Other reagents with same CAS 89639-36-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 142.59 g/mol
Formula C₆H₇ClN₂
badge Registry Numbers
MDL Number MFCD12196974
thermostat Physical Properties
Boiling Point 270.3±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.260±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof storage, inert atmosphere

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its ability to enhance selectivity and biological activity. Its structure supports the development of compounds with improved environmental stability and target specificity. Also employed in pharmaceutical research for building nitrogen-containing heterocyclic systems in drug candidates, especially those targeting central nervous system disorders and inflammatory conditions. Commonly utilized in cross-coupling reactions to form C–N or C–C bonds, making it valuable in medicinal chemistry and crop protection agent development.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,040.00
inventory 5g
10-20 days ฿3,090.00
inventory 25g
10-20 days ฿12,310.00
inventory 100g
10-20 days ฿41,190.00

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5-Chloro-2-methyl-pyridin-3-ylamine
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Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its ability to enhance selectivity and biological activity. Its structure supports the development of compounds with improved environmental stability and target specificity. Also employed in pharmaceutical research for building nitrogen-containing heterocyclic systems in drug candidates, especially those targeting central nervous system disorders and inflammatory conditions. Commonly utilized in

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its ability to enhance selectivity and biological activity. Its structure supports the development of compounds with improved environmental stability and target specificity. Also employed in pharmaceutical research for building nitrogen-containing heterocyclic systems in drug candidates, especially those targeting central nervous system disorders and inflammatory conditions. Commonly utilized in cross-coupling reactions to form C–N or C–C bonds, making it valuable in medicinal chemistry and crop protection agent development.

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