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Structure of 6351-10-6
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This bench-stable indenol features a reactive hydroxyl group flanked by a rigid bicyclic framework, enabling straightforward functionalization in synthetic transformations. Its solubility in common organic solvents supports use in catalytic reactions and as a building block for complex molecular architectures.
2,3-Dihydro-1H-inden-1-ol serves as a versatile building block in synthetic organic chemistry, offering a rigid, chiral scaffold with a primary hydroxyl group. Its functionality enables straightforward derivatization via esterification, etherification, and oxidation to the corresponding aldehyde or carboxylic acid. The compound exhibits good bench stability and is compatible with standard protecting group strategies, facilitating its use in complex molecule synthesis, including heterocyclic systems and natural product analogs.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: