(S)-Styrene oxide

98%

Reagent Code: #234724
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CAS Number 20780-54-5

science Other reagents with same CAS 20780-54-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 120.15 g/mol
Formula C₈H₈O
badge Registry Numbers
MDL Number MFCD00064310
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Used as a key chiral building block in the synthesis of pharmaceuticals, particularly in the production of β-blockers like (S)-propranolol and other active pharmaceutical ingredients where stereochemistry is critical. Its epoxide ring readily undergoes nucleophilic opening, enabling the introduction of functional groups in a stereoselective manner. Also employed in the preparation of fine chemicals, agrochemicals, and chiral ligands for asymmetric catalysis. Due to its enantiomeric purity, it plays a vital role in routes requiring high optical selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿910.00
inventory 100g
10-20 days ฿11,470.00
inventory 25g
10-20 days ฿3,200.00
(S)-Styrene oxide
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Used as a key chiral building block in the synthesis of pharmaceuticals, particularly in the production of β-blockers like (S)-propranolol and other active pharmaceutical ingredients where stereochemistry is critical. Its epoxide ring readily undergoes nucleophilic opening, enabling the introduction of functional groups in a stereoselective manner. Also employed in the preparation of fine chemicals, agrochemicals, and chiral ligands for asymmetric catalysis. Due to its enantiomeric purity, it plays a vit

Used as a key chiral building block in the synthesis of pharmaceuticals, particularly in the production of β-blockers like (S)-propranolol and other active pharmaceutical ingredients where stereochemistry is critical. Its epoxide ring readily undergoes nucleophilic opening, enabling the introduction of functional groups in a stereoselective manner. Also employed in the preparation of fine chemicals, agrochemicals, and chiral ligands for asymmetric catalysis. Due to its enantiomeric purity, it plays a vital role in routes requiring high optical selectivity.

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