(S)-2-(2, 6-Dichlorobenzamido)succinic acid

97%

Reagent Code: #236482
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CAS Number 1786734-56-2

science Other reagents with same CAS 1786734-56-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.10 g/mol
Formula C₁₁H₉Cl₂NO₅
badge Registry Numbers
MDL Number MFCD23149070
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a chiral resolving agent in the pharmaceutical industry for the separation of enantiomers, particularly in the production of optically active drugs. Its stereochemical purity allows efficient resolution of racemic mixtures through diastereomeric salt formation. Commonly applied in the synthesis of angiotensin-converting enzyme (ACE) inhibitors and other bioactive molecules where enantiomeric purity is critical. Also utilized in asymmetric synthesis as a chiral auxiliary to control stereochemistry in complex organic transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿8,870.00
inventory 100mg
10-20 days ฿13,320.00
inventory 250mg
10-20 days ฿19,980.00
(S)-2-(2, 6-Dichlorobenzamido)succinic acid
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Used as a chiral resolving agent in the pharmaceutical industry for the separation of enantiomers, particularly in the production of optically active drugs. Its stereochemical purity allows efficient resolution of racemic mixtures through diastereomeric salt formation. Commonly applied in the synthesis of angiotensin-converting enzyme (ACE) inhibitors and other bioactive molecules where enantiomeric purity is critical. Also utilized in asymmetric synthesis as a chiral auxiliary to control stereochemistry

Used as a chiral resolving agent in the pharmaceutical industry for the separation of enantiomers, particularly in the production of optically active drugs. Its stereochemical purity allows efficient resolution of racemic mixtures through diastereomeric salt formation. Commonly applied in the synthesis of angiotensin-converting enzyme (ACE) inhibitors and other bioactive molecules where enantiomeric purity is critical. Also utilized in asymmetric synthesis as a chiral auxiliary to control stereochemistry in complex organic transformations.

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