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Structure of 886372-05-0
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Methyl 4-chloro-6-methylnicotinate is a bench-stable, electron-deficient heterocyclic ester featuring a chlorine substituent at the 4-position and a methyl group at the 6-position. This configuration enhances regioselectivity in cross-coupling reactions and facilitates direct functionalization of the pyridine ring. The compound serves as a key building block for bioactive nitrogen-containing scaffolds in medicinal chemistry and agrochemical development.
Methyl 4-chloro-6-methylnicotinate serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. Its ortho-chloro and methyl substituents enable selective functionalization and facilitate downstream coupling reactions, including Suzuki-Miyaura and Buchwald-Hartwig transformations. The ester group offers stability and ease of purification, while the pyridine core provides a robust scaffold for drug-like molecule development.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: