4-Amino-6-chloronicotinaldehyde

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Reagent Code: #136939
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CAS Number 1001756-21-3

science Other reagents with same CAS 1001756-21-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 156.57 g/mol
Formula C₆H₅ClN₂O
badge Registry Numbers
MDL Number MFCD09834660
thermostat Physical Properties
Boiling Point 379°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and plant growth regulators. Its aldehyde and amino functional groups allow for versatile chemical modifications, making it valuable in constructing nitrogen-containing heterocyclic compounds. It is also employed in the development of active ingredients in crop protection agents due to its reactivity and selectivity in coupling reactions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,140.00
inventory 1g
10-20 days ฿2,400.00
inventory 5g
10-20 days ฿10,660.00
inventory 25g
10-20 days ฿38,400.00

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4-Amino-6-chloronicotinaldehyde
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and plant growth regulators. Its aldehyde and amino functional groups allow for versatile chemical modifications, making it valuable in constructing nitrogen-containing heterocyclic compounds. It is also employed in the development of active ingredients in crop protection agents due to its reactivity and selectivity in coupling reactions.

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and plant growth regulators. Its aldehyde and amino functional groups allow for versatile chemical modifications, making it valuable in constructing nitrogen-containing heterocyclic compounds. It is also employed in the development of active ingredients in crop protection agents due to its reactivity and selectivity in coupling reactions.

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