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Structure of 100836-85-9
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(R)-(+)-2-Benzyloxypropionic acid features a chiral center with defined stereochemistry, enabling precise incorporation into asymmetric synthesis. The benzyloxy group provides enhanced stability and selective reactivity under standard conditions. This bench-stable derivative serves as a key building block for pharmaceutical intermediates and functionalized polymers.
(R)-(+)-2-Benzyloxypropionic acid serves as a valuable chiral building block for the synthesis of bioactive molecules and pharmaceutical intermediates. Its well-defined stereochemistry enables stereoselective transformations, while the benzyloxy group provides orthogonal protection for carboxylic acid functionalities. The compound exhibits excellent bench stability and facilitates straightforward purification, making it suitable for use in multi-step synthetic sequences involving esterifications, amide couplings, or further functionalization under standard organic reaction conditions.
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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: