(2R,3R)-Dimethyl 2,3-bis((4-methylbenzoyl)oxy)succinate

95%

Reagent Code: #229473
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CAS Number 2703746-29-4

science Other reagents with same CAS 2703746-29-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 414.41 g/mol
Formula C₂₂H₂₂O₈
badge Registry Numbers
MDL Number MFCD27578184
thermostat Physical Properties
Boiling Point 544.4±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.246±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a chiral derivatizing agent in stereochemical analysis, particularly in the determination of enantiomeric purity of chiral alcohols and amines. Its rigid structure and two ester functionalities allow it to form diastereomeric esters with enantiomers, which can then be separated and analyzed using techniques like HPLC or NMR. The presence of aromatic groups enhances detectability by UV detection. Commonly applied in pharmaceutical research for resolving racemic mixtures and validating asymmetric synthesis pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,240.00
inventory 250mg
10-20 days ฿10,850.00
inventory 1g
10-20 days ฿29,380.00

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(2R,3R)-Dimethyl 2,3-bis((4-methylbenzoyl)oxy)succinate
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Used as a chiral derivatizing agent in stereochemical analysis, particularly in the determination of enantiomeric purity of chiral alcohols and amines. Its rigid structure and two ester functionalities allow it to form diastereomeric esters with enantiomers, which can then be separated and analyzed using techniques like HPLC or NMR. The presence of aromatic groups enhances detectability by UV detection. Commonly applied in pharmaceutical research for resolving racemic mixtures and validating asymmetric s

Used as a chiral derivatizing agent in stereochemical analysis, particularly in the determination of enantiomeric purity of chiral alcohols and amines. Its rigid structure and two ester functionalities allow it to form diastereomeric esters with enantiomers, which can then be separated and analyzed using techniques like HPLC or NMR. The presence of aromatic groups enhances detectability by UV detection. Commonly applied in pharmaceutical research for resolving racemic mixtures and validating asymmetric synthesis pathways.

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