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Structure of 933717-10-3
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1H-Pyrrolo[3,2-c]pyridine-3-carboxaldehyde features a fused heterocyclic core with a strategically positioned aldehyde group, enabling direct functionalization in transition metal-catalyzed couplings and multicomponent reactions. The electron-deficient pyrrole ring enhances reactivity in electrophilic transformations, while the aldehyde serves as a key handle for conjugation. This scaffold supports rapid access to bioactive molecules in medicinal chemistry and materials science applications.
1H-Pyrrolo[3,2-c]pyridine-3-carboxaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient construction of heterocyclic scaffolds via standard aldehyde transformations. Its conjugated system imparts stability and facilitates electrophilic reactions, while the aldehyde group supports reductive amination, cyanation, and coupling protocols. The molecule exhibits excellent bench stability and is compatible with common protecting group strategies, making it ideal for iterative synthesis campaigns in API 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: