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Structure of 118768-13-1
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Pyrrolo[1,2-b]pyridazine-6-carboxylic acid features a fused heterocyclic core with a carboxylic acid at the 6-position, enabling direct conjugation or derivatization. This scaffold combines electron-deficient aromaticity with a polar functional group, enhancing solubility and facilitating integration into bioactive molecules and medicinal chemistry libraries.
Pyrrolo[1,2-b]pyridazine-6-carboxylic acid serves as a versatile heterocyclic building block for medicinal chemistry and agrochemical research. Its rigid fused scaffold offers enhanced metabolic stability and facilitates hydrogen bonding in target binding pockets. The carboxylic acid group enables straightforward derivatization via amide coupling, esterification, or salt formation, supporting diverse functionalization strategies. Bench-stable and compatible with standard purification methods, it functions reliably in multi-step syntheses and scale-up processes.
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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: