(S)-(-)-N-(1-Phenylethyl)succinamic acid

≥97%

Reagent Code: #237877
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CAS Number 21752-34-1

science Other reagents with same CAS 21752-34-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.25 g/mol
Formula C₁₂H₁₅NO₃
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MDL Number MFCD00077433
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a chiral resolving agent in the separation of enantiomers, particularly in the resolution of racemic mixtures of carboxylic acids and amines. Its structural features allow it to form diastereomeric salts with chiral acids or bases, which can be separated based on differences in solubility or crystallization behavior. Commonly applied in asymmetric synthesis and pharmaceutical intermediate purification where enantiomeric purity is critical. Also employed in the development of chiral stationary phases for chromatography due to its ability to discriminate between enantiomers.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,260.00
inventory 250mg
10-20 days ฿13,010.00
(S)-(-)-N-(1-Phenylethyl)succinamic acid
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Used as a chiral resolving agent in the separation of enantiomers, particularly in the resolution of racemic mixtures of carboxylic acids and amines. Its structural features allow it to form diastereomeric salts with chiral acids or bases, which can be separated based on differences in solubility or crystallization behavior. Commonly applied in asymmetric synthesis and pharmaceutical intermediate purification where enantiomeric purity is critical. Also employed in the development of chiral stationary pha

Used as a chiral resolving agent in the separation of enantiomers, particularly in the resolution of racemic mixtures of carboxylic acids and amines. Its structural features allow it to form diastereomeric salts with chiral acids or bases, which can be separated based on differences in solubility or crystallization behavior. Commonly applied in asymmetric synthesis and pharmaceutical intermediate purification where enantiomeric purity is critical. Also employed in the development of chiral stationary phases for chromatography due to its ability to discriminate between enantiomers.

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