(S)-Azetidin-2-ylmethanol

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Reagent Code: #233537
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CAS Number 104587-62-4

science Other reagents with same CAS 104587-62-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 87.12 g/mol
Formula C₄H₉NO
badge Registry Numbers
MDL Number MFCD10565790
thermostat Physical Properties
Boiling Point 151.9±13.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.017±0.06 g/cm3(Predicted)
Storage 2-8°C, away from light, dry

description Product Description

Used as a chiral building block in the synthesis of β-lactam antibiotics, particularly in the production of penem and carbapenem classes. Its strained azetidine ring and hydroxymethyl group enable selective functionalization for constructing complex antibiotic scaffolds. The (S)-configuration is critical for biological activity in final drug compounds. Also employed in medicinal chemistry for developing enzyme inhibitors and other bioactive molecules where stereochemistry influences potency.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,920.00
inventory 250mg
10-20 days ฿16,550.00
inventory 1g
10-20 days ฿33,100.00

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(S)-Azetidin-2-ylmethanol
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Used as a chiral building block in the synthesis of β-lactam antibiotics, particularly in the production of penem and carbapenem classes. Its strained azetidine ring and hydroxymethyl group enable selective functionalization for constructing complex antibiotic scaffolds. The (S)-configuration is critical for biological activity in final drug compounds. Also employed in medicinal chemistry for developing enzyme inhibitors and other bioactive molecules where stereochemistry influences potency.

Used as a chiral building block in the synthesis of β-lactam antibiotics, particularly in the production of penem and carbapenem classes. Its strained azetidine ring and hydroxymethyl group enable selective functionalization for constructing complex antibiotic scaffolds. The (S)-configuration is critical for biological activity in final drug compounds. Also employed in medicinal chemistry for developing enzyme inhibitors and other bioactive molecules where stereochemistry influences potency.

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