(S)-()-3-(BENZYLOXYCARBONYL)-5-OXO-4-OXAZOLIDINEPROPIONIC ACID

97%

Reagent Code: #235914
fingerprint
CAS Number 23632-67-9

science Other reagents with same CAS 23632-67-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.27 g/mol
Formula C₁₄H₁₅NO₆
thermostat Physical Properties
Melting Point 68-69 °C
Boiling Point 557.2±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.05 g/mL at 25 °C(lit.)
Storage -20°C

description Product Description

Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of β-lactam antibiotics. It facilitates stereocontrol during carbon-carbon bond formation, enabling the efficient synthesis of optically active intermediates. Commonly employed in the pharmaceutical industry for the production of penem and carbapenem class antibiotics due to its ability to direct stereoselective alkylation reactions. Also utilized in peptide mimetic synthesis where preservation of chirality is critical. Its cyclic structure and activating groups allow for selective transformations and easy removal under mild conditions, making it valuable in multi-step synthetic routes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,100.00
inventory 1g
10-20 days ฿18,700.00
inventory 5g
10-20 days ฿65,370.00
(S)-()-3-(BENZYLOXYCARBONYL)-5-OXO-4-OXAZOLIDINEPROPIONIC ACID
No image available

Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of β-lactam antibiotics. It facilitates stereocontrol during carbon-carbon bond formation, enabling the efficient synthesis of optically active intermediates. Commonly employed in the pharmaceutical industry for the production of penem and carbapenem class antibiotics due to its ability to direct stereoselective alkylation reactions. Also utilized in peptide mimetic synthesis where preservation of chirality is critical. I

Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of β-lactam antibiotics. It facilitates stereocontrol during carbon-carbon bond formation, enabling the efficient synthesis of optically active intermediates. Commonly employed in the pharmaceutical industry for the production of penem and carbapenem class antibiotics due to its ability to direct stereoselective alkylation reactions. Also utilized in peptide mimetic synthesis where preservation of chirality is critical. Its cyclic structure and activating groups allow for selective transformations and easy removal under mild conditions, making it valuable in multi-step synthetic routes.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...