(2S,4R)-3-(tert-Butoxycarbonyl)-2-(tert-butyl)-4-methyloxazolidine-4-carboxylic acid

95%

Reagent Code: #236006
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CAS Number 1686957-60-7

science Other reagents with same CAS 1686957-60-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.35 g/mol
Formula C₁₄H₂₅NO₅
thermostat Physical Properties
Boiling Point 387.4±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.127±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a chiral auxiliary or intermediate in asymmetric synthesis, particularly in the pharmaceutical industry for the preparation of enantiomerically pure compounds. Its rigid oxazolidine ring structure helps control stereochemistry during key bond-forming reactions, such as alkylations, aldol additions, or reductions. The tert-butoxycarbonyl and tert-butyl groups provide steric bulk and stability, facilitating high diastereoselectivity. After serving its purpose, the auxiliary can be cleaved under mild acidic conditions, leaving the desired chiral product intact. Commonly employed in the synthesis of complex bioactive molecules, including protease inhibitors and other therapeutic agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,250.00
inventory 1g
10-20 days ฿49,880.00

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(2S,4R)-3-(tert-Butoxycarbonyl)-2-(tert-butyl)-4-methyloxazolidine-4-carboxylic acid
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Used as a chiral auxiliary or intermediate in asymmetric synthesis, particularly in the pharmaceutical industry for the preparation of enantiomerically pure compounds. Its rigid oxazolidine ring structure helps control stereochemistry during key bond-forming reactions, such as alkylations, aldol additions, or reductions. The tert-butoxycarbonyl and tert-butyl groups provide steric bulk and stability, facilitating high diastereoselectivity. After serving its purpose, the auxiliary can be cleaved under mil

Used as a chiral auxiliary or intermediate in asymmetric synthesis, particularly in the pharmaceutical industry for the preparation of enantiomerically pure compounds. Its rigid oxazolidine ring structure helps control stereochemistry during key bond-forming reactions, such as alkylations, aldol additions, or reductions. The tert-butoxycarbonyl and tert-butyl groups provide steric bulk and stability, facilitating high diastereoselectivity. After serving its purpose, the auxiliary can be cleaved under mild acidic conditions, leaving the desired chiral product intact. Commonly employed in the synthesis of complex bioactive molecules, including protease inhibitors and other therapeutic agents.

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