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Structure of 66093-07-0
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5,6-Dimethylpyridin-3-amine features a pyridine core with methyl groups at the 5 and 6 positions, enhancing electron density at the nitrogen lone pair. This substitution pattern improves basicity and solubility in organic media while maintaining bench-stability. The molecule serves as a robust ligand in transition metal catalysis and a key scaffold in medicinal chemistry due to its ability to engage in hydrogen bonding and π-stacking interactions.
5,6-Dimethylpyridin-3-amine serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles through standard coupling and functionalization reactions. Its electron-rich pyridine core exhibits enhanced nucleophilicity compared to unsubstituted analogs, facilitating efficient derivatization under mild conditions. The dimethyl substitution pattern provides steric and electronic tuning for improved metabolic stability and target engagement, while the amine functionality offers a direct handle for conjugation or salt formation. Bench-stable and readily purified, it functions effectively in both small-molecule synthesis and high-throughput screening campaigns.
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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: