(R)-tert-Butyl 4-(bromomethyl)-2,2-dimethyloxazolidine-3-carboxylate

95%

Reagent Code: #37671
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CAS Number 1260610-79-4

science Other reagents with same CAS 1260610-79-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.1854 g/mol
Formula C₁₁H₂₀BrNO₃
badge Registry Numbers
MDL Number MFCD09863821
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis as a chiral building block for the preparation of complex molecules. It is particularly valuable in the synthesis of enantiomerically pure compounds, especially in the pharmaceutical industry, where it aids in the development of drugs with specific stereochemical requirements. The bromomethyl group allows for further functionalization, making it a versatile intermediate in the construction of various biologically active molecules. Additionally, its oxazolidine ring provides stability and can act as a protecting group for amines during multi-step synthetic processes.

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inventory 100mg
10-20 days ฿4,680.00

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(R)-tert-Butyl 4-(bromomethyl)-2,2-dimethyloxazolidine-3-carboxylate
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This compound is primarily utilized in organic synthesis as a chiral building block for the preparation of complex molecules. It is particularly valuable in the synthesis of enantiomerically pure compounds, especially in the pharmaceutical industry, where it aids in the development of drugs with specific stereochemical requirements. The bromomethyl group allows for further functionalization, making it a versatile intermediate in the construction of various biologically active molecules. Additionally, its

This compound is primarily utilized in organic synthesis as a chiral building block for the preparation of complex molecules. It is particularly valuable in the synthesis of enantiomerically pure compounds, especially in the pharmaceutical industry, where it aids in the development of drugs with specific stereochemical requirements. The bromomethyl group allows for further functionalization, making it a versatile intermediate in the construction of various biologically active molecules. Additionally, its oxazolidine ring provides stability and can act as a protecting group for amines during multi-step synthetic processes.

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