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Structure of 823-61-0
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3,6-Dimethyl-2-pyridinamine features a pyridine core with methyl groups at the 3 and 6 positions, enhancing electron density at the nitrogen lone pair. This bench-stable derivative serves as a selective ligand in transition metal catalysis, offering improved solubility and reduced basicity compared to unsubstituted analogs.
3,6-Dimethyl-2-pyridinamine serves as a versatile building block in medicinal chemistry and catalysis, offering enhanced electronic modulation via its methyl-substituted pyridine core. The primary amine functionality enables straightforward derivatization, while the steric and electronic profile supports use in transition metal-catalyzed coupling reactions and heterocyclic scaffold construction. Bench-stable and readily purified, it functions effectively in standard synthetic workflows for API development and ligand design.
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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: