(R)-tert-Butyl (2-(4-bromophenyl)propyl)carbamate

97%

Reagent Code: #37279
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CAS Number 211315-53-6

science Other reagents with same CAS 211315-53-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 314.2300 g/mol
Formula C₁₄H₂₀BrNO₂
badge Registry Numbers
MDL Number MFCD28334223
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the production of chiral molecules, which are essential for creating enantiomerically pure drugs. Its structure, featuring a bromophenyl group and a tert-butyl carbamate moiety, makes it valuable for constructing complex organic frameworks. The compound is often employed in the synthesis of biologically active molecules, including potential therapeutic agents targeting neurological disorders or other medical conditions. Additionally, it is used in research settings to study stereochemistry and reaction mechanisms, aiding in the advancement of synthetic methodologies.

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Test Parameter Specification
Appearance White to off-white Solid
Purity (%) 96.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿378.00

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(R)-tert-Butyl (2-(4-bromophenyl)propyl)carbamate
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This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the production of chiral molecules, which are essential for creating enantiomerically pure drugs. Its structure, featuring a bromophenyl group and a tert-butyl carbamate moiety, makes it valuable for constructing complex organic frameworks. The compound is often employed in the synthesis of biologically active molecules, including potential therapeutic agents targeting neurological disorders or other medical conditions. Additionally, it is used in research settings to study stereochemistry and reaction mechanisms, aiding in the advancement of synthetic methodologies.
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