(S)-2-(Benzo[b]thiophen-2-yl)-4-ethyl-4,5-dihydrooxazole

97%

Reagent Code: #237477
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CAS Number 2828438-80-6

science Other reagents with same CAS 2828438-80-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.31 g/mol
Formula C₁₃H₁₃NOS
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, inert gas

description Product Description

Used as a chiral auxiliary in asymmetric synthesis, this compound plays a key role in controlling stereochemistry during the formation of carbon-carbon bonds. It is particularly effective in enantioselective alkylation reactions, where it helps generate optically active intermediates for pharmaceuticals. Due to its rigid structure and coordination properties, it facilitates high enantiomeric excess in products. Commonly employed in the synthesis of bioactive molecules, it enables efficient construction of complex organic frameworks, especially in medicinal chemistry and natural product synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,580.00
inventory 1g
10-20 days ฿30,820.00
inventory 250mg
10-20 days ฿8,180.00
(S)-2-(Benzo[b]thiophen-2-yl)-4-ethyl-4,5-dihydrooxazole
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Used as a chiral auxiliary in asymmetric synthesis, this compound plays a key role in controlling stereochemistry during the formation of carbon-carbon bonds. It is particularly effective in enantioselective alkylation reactions, where it helps generate optically active intermediates for pharmaceuticals. Due to its rigid structure and coordination properties, it facilitates high enantiomeric excess in products. Commonly employed in the synthesis of bioactive molecules, it enables efficient construction of c
Used as a chiral auxiliary in asymmetric synthesis, this compound plays a key role in controlling stereochemistry during the formation of carbon-carbon bonds. It is particularly effective in enantioselective alkylation reactions, where it helps generate optically active intermediates for pharmaceuticals. Due to its rigid structure and coordination properties, it facilitates high enantiomeric excess in products. Commonly employed in the synthesis of bioactive molecules, it enables efficient construction of complex organic frameworks, especially in medicinal chemistry and natural product synthesis.
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