(R)-tert-Butyl 4-(3-bromoprop-1-en-1-yl)-2,2-dimethyloxazolidine-3-carboxylate[R-(E)]-
97%
Reagent
Code: #228776
CAS Number
142573-55-5
science Other reagents with same CAS 142573-55-5
blur_circular Chemical Specifications
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Molecular Information
Weight
320.22 g/mol
Formula
C₁₃H₂₂BrNO₃
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Registry Numbers
MDL Number
MFCD26406788
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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.