Methyl 2-amino-5-chloronicotinate

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Reagent Code: #205977
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CAS Number 50735-33-6

science Other reagents with same CAS 50735-33-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.59 g/mol
Formula C₇H₇ClN₂O₂
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its structure supports the creation of compounds with chloro-substituted pyridine rings, which are common in modern crop protection agents. Also employed in medicinal chemistry for building blocks in kinase inhibitors and other bioactive molecules. The amine and ester functional groups allow for easy modification, making it valuable in combinatorial chemistry and drug discovery research.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿860.00
inventory 5g
10-20 days ฿4,100.00
inventory 10g
10-20 days ฿8,190.00
inventory 25g
10-20 days ฿17,780.00
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Methyl 2-amino-5-chloronicotinate
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its structure supports the creation of compounds with chloro-substituted pyridine rings, which are common in modern crop protection agents. Also employed in medicinal chemistry for building blocks in kinase inhibitors and other bioactive molecules. The amine and ester functional groups allow for easy modification, making it valuable in combinatorial

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its structure supports the creation of compounds with chloro-substituted pyridine rings, which are common in modern crop protection agents. Also employed in medicinal chemistry for building blocks in kinase inhibitors and other bioactive molecules. The amine and ester functional groups allow for easy modification, making it valuable in combinatorial chemistry and drug discovery research.

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