(S)-2-(2-bromophenyl)-4-(tert-butyl)-4,5-dihydrooxazole

97%

Reagent Code: #236088
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CAS Number 154701-60-7

science Other reagents with same CAS 154701-60-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 282.18 g/mol
Formula C₁₃H₁₆BrNO
badge Registry Numbers
MDL Number MFCD08234769
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral auxiliary in asymmetric synthesis, particularly in enantioselective carbon-carbon bond-forming reactions. Its rigid oxazoline ring and bulky tert-butyl group help control stereochemistry, making it valuable in the preparation of optically active pharmaceuticals and fine chemicals. The bromophenyl moiety allows for further functionalization via cross-coupling reactions, enabling the construction of complex molecular architectures. Commonly employed in catalysis and medicinal chemistry research for developing enantiopure intermediates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,280.00
inventory 1g
10-20 days ฿10,900.00
(S)-2-(2-bromophenyl)-4-(tert-butyl)-4,5-dihydrooxazole
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Used as a chiral auxiliary in asymmetric synthesis, particularly in enantioselective carbon-carbon bond-forming reactions. Its rigid oxazoline ring and bulky tert-butyl group help control stereochemistry, making it valuable in the preparation of optically active pharmaceuticals and fine chemicals. The bromophenyl moiety allows for further functionalization via cross-coupling reactions, enabling the construction of complex molecular architectures. Commonly employed in catalysis and medicinal chemistry resear
Used as a chiral auxiliary in asymmetric synthesis, particularly in enantioselective carbon-carbon bond-forming reactions. Its rigid oxazoline ring and bulky tert-butyl group help control stereochemistry, making it valuable in the preparation of optically active pharmaceuticals and fine chemicals. The bromophenyl moiety allows for further functionalization via cross-coupling reactions, enabling the construction of complex molecular architectures. Commonly employed in catalysis and medicinal chemistry research for developing enantiopure intermediates.
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