(R)-()-2-Acetoxysuccinic anhydride

≥97%

Reagent Code: #230260
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CAS Number 79814-40-7

science Other reagents with same CAS 79814-40-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.11 g/mol
Formula C₆H₆O₅
badge Registry Numbers
MDL Number MFCD00145214
thermostat Physical Properties
Melting Point 56-58 °C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a chiral derivatizing agent in the synthesis of optically active compounds, particularly in the preparation of enantiomerically pure pharmaceuticals. Its asymmetric structure allows selective acylation in peptide and beta-lactam synthesis, making it valuable in developing antibiotics and other bioactive molecules. Also employed in resolving racemic mixtures due to its ability to form diastereomeric intermediates that can be easily separated. Commonly applied in research settings for stereocontrolled synthesis where high enantiomeric excess is required.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,660.00
5g
10-20 days ฿4,100.00
25g
10-20 days ฿17,190.00
(R)-()-2-Acetoxysuccinic anhydride
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Used as a chiral derivatizing agent in the synthesis of optically active compounds, particularly in the preparation of enantiomerically pure pharmaceuticals. Its asymmetric structure allows selective acylation in peptide and beta-lactam synthesis, making it valuable in developing antibiotics and other bioactive molecules. Also employed in resolving racemic mixtures due to its ability to form diastereomeric intermediates that can be easily separated. Commonly applied in research settings for stereocontrol

Used as a chiral derivatizing agent in the synthesis of optically active compounds, particularly in the preparation of enantiomerically pure pharmaceuticals. Its asymmetric structure allows selective acylation in peptide and beta-lactam synthesis, making it valuable in developing antibiotics and other bioactive molecules. Also employed in resolving racemic mixtures due to its ability to form diastereomeric intermediates that can be easily separated. Commonly applied in research settings for stereocontrolled synthesis where high enantiomeric excess is required.

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