(S)-tert-Butyl (1-(2-bromophenyl)ethyl)carbamate

≥95%

Reagent Code: #113633
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CAS Number 1187932-11-1

science Other reagents with same CAS 1187932-11-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 300.19 g/mol
Formula C₁₃H₁₈BrNO₂
badge Registry Numbers
MDL Number MFCD11506016
thermostat Physical Properties
Boiling Point 375.2±25.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. It is particularly valuable in the pharmaceutical industry for the development of chiral compounds, where its stereochemistry plays a crucial role in creating enantiomerically pure drugs. The presence of the bromophenyl group allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, making it a versatile building block in medicinal chemistry. Additionally, the tert-butyl carbamate group provides a protective function for amines, enabling selective reactions in multi-step synthetic processes. Its application is also seen in the synthesis of biologically active compounds, including potential therapeutic agents targeting neurological disorders or cancer.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,851.00
inventory 250mg
10-20 days ฿7,281.00
inventory 1g
10-20 days ฿16,731.00

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(S)-tert-Butyl (1-(2-bromophenyl)ethyl)carbamate
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This chemical is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. It is particularly valuable in the pharmaceutical industry for the development of chiral compounds, where its stereochemistry plays a crucial role in creating enantiomerically pure drugs. The presence of the bromophenyl group allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, making it a versatile building block in medicinal chemistry

This chemical is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. It is particularly valuable in the pharmaceutical industry for the development of chiral compounds, where its stereochemistry plays a crucial role in creating enantiomerically pure drugs. The presence of the bromophenyl group allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, making it a versatile building block in medicinal chemistry. Additionally, the tert-butyl carbamate group provides a protective function for amines, enabling selective reactions in multi-step synthetic processes. Its application is also seen in the synthesis of biologically active compounds, including potential therapeutic agents targeting neurological disorders or cancer.

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