(R)-tert-Butyl 4-(3-bromoprop-1-en-1-yl)-2,2-dimethyloxazolidine-3-carboxylate[R-(E)]-

97%

Reagent Code: #228776
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CAS Number 142573-55-5

science Other reagents with same CAS 142573-55-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 320.22 g/mol
Formula C₁₃H₂₂BrNO₃
badge Registry Numbers
MDL Number MFCD26406788
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of complex organic molecules, particularly in pharmaceuticals where stereochemistry is critical. Its structure allows for selective introduction of functional groups in asymmetric synthesis. The bromoalkene moiety serves as a versatile handle for cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of carbon-carbon bonds. The oxazolidine ring acts as a protecting group for amines and also directs stereoselectivity in subsequent transformations. Commonly employed in the development of bioactive compounds, including potential drug candidates in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,930.00
inventory 250mg
10-20 days ฿11,980.00
inventory 500mg
10-20 days ฿19,980.00
(R)-tert-Butyl 4-(3-bromoprop-1-en-1-yl)-2,2-dimethyloxazolidine-3-carboxylate[R-(E)]-
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Used as a chiral building block in the synthesis of complex organic molecules, particularly in pharmaceuticals where stereochemistry is critical. Its structure allows for selective introduction of functional groups in asymmetric synthesis. The bromoalkene moiety serves as a versatile handle for cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of carbon-carbon bonds. The oxazolidine ring acts as a protecting group for amines and also directs stereoselectivity in subsequent transformations. Commonly employed in the development of bioactive compounds, including potential drug candidates in medicinal chemistry research.
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