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Structure of 1730-92-3
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(S)-3-Methylpentanoic acid is a chiral carboxylic acid featuring a branched alkyl chain with defined stereochemistry at the 3-position. This configuration imparts distinct conformational and reactivity profiles, making it valuable for asymmetric synthesis and the construction of enantiopure pharmaceutical intermediates. The molecule exhibits enhanced solubility in organic solvents and stability under standard bench conditions, facilitating straightforward handling in synthetic workflows.
(S)-3-Methylpentanoic acid serves as a chiral building block for the synthesis of bioactive molecules and pharmaceutical intermediates. Its well-defined stereochemistry enables stereoselective transformations in medicinal chemistry, while the aliphatic chain supports compatibility with standard functional group manipulations. The compound exhibits bench stability and facilitates efficient derivatization via esterification, amidation, or reduction, making it a practical choice for route optimization 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-H319
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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: