(R)-tert-Butyl (1-(3-bromophenyl)-2-hydroxyethyl)carbamate

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Reagent Code: #113420
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CAS Number 380610-92-4

science Other reagents with same CAS 380610-92-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 316.19 g/mol
Formula C₁₃H₁₈BrNO₃
badge Registry Numbers
MDL Number MFCD27978721
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules, particularly in the pharmaceutical industry. Its structure, featuring a bromophenyl group and a carbamate moiety, makes it valuable for constructing biologically active compounds, such as inhibitors or receptor modulators. The presence of the tert-butyl group enhances stability during synthetic processes, while the hydroxyl group provides a reactive site for further functionalization. It is often employed in the development of chiral drugs due to its (R)-configuration, which is crucial for achieving specific stereochemical outcomes in drug design. Additionally, the bromine atom serves as a handle for cross-coupling reactions, enabling the introduction of diverse substituents to tailor the compound's properties for targeted applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿711.00
inventory 250mg
10-20 days ฿1,188.00
inventory 1g
10-20 days ฿3,546.00

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(R)-tert-Butyl (1-(3-bromophenyl)-2-hydroxyethyl)carbamate
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This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules, particularly in the pharmaceutical industry. Its structure, featuring a bromophenyl group and a carbamate moiety, makes it valuable for constructing biologically active compounds, such as inhibitors or receptor modulators. The presence of the tert-butyl group enhances stability during synthetic processes, while the hydroxyl group provides a reactive site for further functionalization

This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules, particularly in the pharmaceutical industry. Its structure, featuring a bromophenyl group and a carbamate moiety, makes it valuable for constructing biologically active compounds, such as inhibitors or receptor modulators. The presence of the tert-butyl group enhances stability during synthetic processes, while the hydroxyl group provides a reactive site for further functionalization. It is often employed in the development of chiral drugs due to its (R)-configuration, which is crucial for achieving specific stereochemical outcomes in drug design. Additionally, the bromine atom serves as a handle for cross-coupling reactions, enabling the introduction of diverse substituents to tailor the compound's properties for targeted applications.

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