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

95%

Reagent Code: #233254
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CAS Number 2828438-78-2

science Other reagents with same CAS 2828438-78-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.37 g/mol
Formula C₁₅H₁₇NOS
thermostat Physical Properties
Boiling Point 398.5±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.22±0.1 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

Used as a chiral intermediate in the synthesis of active pharmaceutical ingredients, particularly in the development of enantiomerically pure drugs. Its oxazole ring and benzo[b]thiophene moiety contribute to binding selectivity in biological targets, making it valuable in medicinal chemistry for designing protease inhibitors and anti-inflammatory agents. Also employed in asymmetric synthesis due to its stereochemical stability and ability to direct stereoselective transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,810.00
inventory 250mg
10-20 days ฿8,180.00

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(S)-2-(Benzo[b]thiophen-2-yl)-4-isobutyl-4,5-dihydrooxazole
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Used as a chiral intermediate in the synthesis of active pharmaceutical ingredients, particularly in the development of enantiomerically pure drugs. Its oxazole ring and benzo[b]thiophene moiety contribute to binding selectivity in biological targets, making it valuable in medicinal chemistry for designing protease inhibitors and anti-inflammatory agents. Also employed in asymmetric synthesis due to its stereochemical stability and ability to direct stereoselective transformations.

Used as a chiral intermediate in the synthesis of active pharmaceutical ingredients, particularly in the development of enantiomerically pure drugs. Its oxazole ring and benzo[b]thiophene moiety contribute to binding selectivity in biological targets, making it valuable in medicinal chemistry for designing protease inhibitors and anti-inflammatory agents. Also employed in asymmetric synthesis due to its stereochemical stability and ability to direct stereoselective transformations.

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