(S)-Oxetane-2-carboxylic acid

97%

Reagent Code: #233166
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CAS Number 2241107-29-7

science Other reagents with same CAS 2241107-29-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 102.09 g/mol
Formula C₄H₆O₃
badge Registry Numbers
MDL Number MFCD31690962
thermostat Physical Properties
Boiling Point 244.2±33.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.374±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used as a chiral building block in pharmaceutical synthesis, particularly in the development of beta-lactam antibiotics. Its strained oxetane ring enhances metabolic stability and improves pharmacokinetic properties in drug candidates. Commonly employed to introduce polarity and rigidity into molecular structures, aiding in the optimization of drug potency and selectivity. Also utilized in the synthesis of protease inhibitors and other bioactive molecules where stereochemistry plays a critical role in activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,030.00
inventory 250mg
10-20 days ฿9,130.00
(S)-Oxetane-2-carboxylic acid
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Used as a chiral building block in pharmaceutical synthesis, particularly in the development of beta-lactam antibiotics. Its strained oxetane ring enhances metabolic stability and improves pharmacokinetic properties in drug candidates. Commonly employed to introduce polarity and rigidity into molecular structures, aiding in the optimization of drug potency and selectivity. Also utilized in the synthesis of protease inhibitors and other bioactive molecules where stereochemistry plays a critical role in ac

Used as a chiral building block in pharmaceutical synthesis, particularly in the development of beta-lactam antibiotics. Its strained oxetane ring enhances metabolic stability and improves pharmacokinetic properties in drug candidates. Commonly employed to introduce polarity and rigidity into molecular structures, aiding in the optimization of drug potency and selectivity. Also utilized in the synthesis of protease inhibitors and other bioactive molecules where stereochemistry plays a critical role in activity.

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