(4S,5R)-3-(tert-Butoxycarbonyl)-2-(4-methoxyphenyl)-4-phenyloxazolidine-5-carboxylic acid

95%

Reagent Code: #235000
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CAS Number 196404-55-4

science Other reagents with same CAS 196404-55-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 399.44 g/mol
Formula C₂₂H₂₅NO₆
thermostat Physical Properties
Melting Point 134-138°C
Boiling Point 573.8°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral auxiliary or intermediate in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds. Its structural features, including the oxazolidine ring with specific substituents and stereochemistry, enable effective stereocontrol during carbon-carbon bond-forming reactions, such as aldol additions. This makes it valuable in the synthesis of complex pharmaceuticals and bioactive molecules containing oxazolidine or related scaffolds. Commonly employed in medicinal chemistry research for developing stereoselective transformations leading to drug candidates and natural product analogs.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,650.00
inventory 10g
10-20 days ฿3,290.00
inventory 25g
10-20 days ฿6,860.00
inventory 100g
10-20 days ฿26,080.00

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(4S,5R)-3-(tert-Butoxycarbonyl)-2-(4-methoxyphenyl)-4-phenyloxazolidine-5-carboxylic acid
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Used as a chiral auxiliary or intermediate in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds. Its structural features, including the oxazolidine ring with specific substituents and stereochemistry, enable effective stereocontrol during carbon-carbon bond-forming reactions, such as aldol additions. This makes it valuable in the synthesis of complex pharmaceuticals and bioactive molecules containing oxazolidine or related scaffolds. Commonly employed in medicinal c

Used as a chiral auxiliary or intermediate in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds. Its structural features, including the oxazolidine ring with specific substituents and stereochemistry, enable effective stereocontrol during carbon-carbon bond-forming reactions, such as aldol additions. This makes it valuable in the synthesis of complex pharmaceuticals and bioactive molecules containing oxazolidine or related scaffolds. Commonly employed in medicinal chemistry research for developing stereoselective transformations leading to drug candidates and natural product analogs.

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