(2R,4S,5R)-3-Boc-2-(4-methoxyphenyl)-4-phenyloxazolidine-5-carboxylic Acid

≥95%

Reagent Code: #231929
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CAS Number 155396-69-3

science Other reagents with same CAS 155396-69-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 399.44 g/mol
Formula C₂₂H₂₅NO₆
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MDL Number MFCD24387546
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds such as pharmaceuticals and natural products. The oxazolidine ring provides stereochemical control during key reactions like aldol additions, alkylations, and Diels-Alder reactions. The Boc (tert-butoxycarbonyl) group allows for easy protection and deprotection of the nitrogen, enabling stepwise synthesis. The 4-methoxyphenyl and phenyl substituents contribute to steric and electronic stabilization of intermediates, enhancing selectivity. Commonly employed in multi-step organic syntheses where high enantioselectivity is required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,230.00
inventory 250mg
10-20 days ฿24,150.00
inventory 1g
10-20 days ฿63,000.00
(2R,4S,5R)-3-Boc-2-(4-methoxyphenyl)-4-phenyloxazolidine-5-carboxylic Acid
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Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds such as pharmaceuticals and natural products. The oxazolidine ring provides stereochemical control during key reactions like aldol additions, alkylations, and Diels-Alder reactions. The Boc (tert-butoxycarbonyl) group allows for easy protection and deprotection of the nitrogen, enabling stepwise synthesis. The 4-methoxyphenyl and phenyl substituents contribute to steric and electronic st

Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds such as pharmaceuticals and natural products. The oxazolidine ring provides stereochemical control during key reactions like aldol additions, alkylations, and Diels-Alder reactions. The Boc (tert-butoxycarbonyl) group allows for easy protection and deprotection of the nitrogen, enabling stepwise synthesis. The 4-methoxyphenyl and phenyl substituents contribute to steric and electronic stabilization of intermediates, enhancing selectivity. Commonly employed in multi-step organic syntheses where high enantioselectivity is required.

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