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Structure of 106778-43-2
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Isoquinoline-6-carboxylic acid serves as a versatile scaffold for medicinal chemistry and materials science, enabling direct functionalization at the 6-position via standard carboxylic acid transformations. Its rigid heteroaromatic core provides enhanced metabolic stability and favorable pharmacokinetic properties in bioactive molecule design. The compound exhibits excellent bench stability, facilitates straightforward derivatization (e.g., amide formation, esterification), and demonstrates broad compatibility with common coupling reagents, making it a practical building block for API development and combinatorial library synthesis.
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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: