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

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Reagent Code: #113845
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CAS Number 910308-92-8

science Other reagents with same CAS 910308-92-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 316.19 g/mol
Formula C₁₃H₁₈BrNO₃
badge Registry Numbers
MDL Number MFCD27952001
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in organic synthesis as a chiral intermediate. Its structure, featuring a bromophenyl group and a hydroxyl group, makes it valuable in the preparation of pharmaceuticals, particularly in the development of enantiomerically pure drugs. The tert-butyl carbamate moiety serves as a protective group for amines, allowing selective reactions to occur at other functional sites. Its application is significant in the synthesis of complex molecules, including those used in neurological and cardiovascular therapies. Additionally, the bromine atom provides a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of diverse chemical architectures.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,251.00
inventory 1g
10-20 days ฿3,168.00
inventory 5g
10-20 days ฿13,185.00

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(S)-tert-Butyl (1-(3-bromophenyl)-2-hydroxyethyl)carbamate
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This compound is primarily utilized in organic synthesis as a chiral intermediate. Its structure, featuring a bromophenyl group and a hydroxyl group, makes it valuable in the preparation of pharmaceuticals, particularly in the development of enantiomerically pure drugs. The tert-butyl carbamate moiety serves as a protective group for amines, allowing selective reactions to occur at other functional sites. Its application is significant in the synthesis of complex molecules, including those used in neurol

This compound is primarily utilized in organic synthesis as a chiral intermediate. Its structure, featuring a bromophenyl group and a hydroxyl group, makes it valuable in the preparation of pharmaceuticals, particularly in the development of enantiomerically pure drugs. The tert-butyl carbamate moiety serves as a protective group for amines, allowing selective reactions to occur at other functional sites. Its application is significant in the synthesis of complex molecules, including those used in neurological and cardiovascular therapies. Additionally, the bromine atom provides a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of diverse chemical architectures.

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