4-chloropyridin-3-amine

98%

Reagent Code: #159380
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CAS Number 20511-15-3

science Other reagents with same CAS 20511-15-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 128.56 g/mol
Formula C₅H₅ClN₂
badge Registry Numbers
MDL Number MFCD00235124
thermostat Physical Properties
Melting Point 58-63 °C
Boiling Point 247.6±20.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.326±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. It serves as a building block in agrochemicals for creating herbicides and pesticides due to its ability to enhance selectivity and reactivity. Also employed in the preparation of functionalized pyridine derivatives used in materials science, including ligands for catalysis and components in organic electronics. Its chlorine and amine groups allow for easy modification through cross-coupling and substitution reactions, making it valuable in medicinal chemistry research.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿1,230.00
25g
10-20 days ฿5,440.00
100g
10-20 days ฿21,260.00
4-chloropyridin-3-amine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. It serves as a building block in agrochemicals for creating herbicides and pesticides due to its ability to enhance selectivity and reactivity. Also employed in the preparation of functionalized pyridine derivatives used in materials science, including ligands for catalysis and components in organic electronics. Its chlorine and amine groups allow for easy modif

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. It serves as a building block in agrochemicals for creating herbicides and pesticides due to its ability to enhance selectivity and reactivity. Also employed in the preparation of functionalized pyridine derivatives used in materials science, including ligands for catalysis and components in organic electronics. Its chlorine and amine groups allow for easy modification through cross-coupling and substitution reactions, making it valuable in medicinal chemistry research.

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