tert-butyl N-(5-bromothiophen-2-yl)carbamate

95%

Reagent Code: #58932
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CAS Number 943321-89-9

science Other reagents with same CAS 943321-89-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.166 g/mol
Formula C₉H₁₂BrNO₂S
badge Registry Numbers
MDL Number MFCD06659527
thermostat Physical Properties
Boiling Point 276.8±25.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. It is often employed in the construction of thiophene-based compounds, which are significant in the pharmaceutical and agrochemical industries. The presence of the bromine atom makes it a valuable building block for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. Additionally, the tert-butyl carbamate group serves as a protective group for amines, allowing selective reactions to occur at other sites of the molecule. This compound is particularly useful in the synthesis of heterocyclic compounds, which are commonly found in drugs and biologically active molecules. Its applications extend to material science, where it can be used to create novel polymers or organic electronic materials.

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Test Parameter Specification
Appearance Light Yellow to Yellow to Grey Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,221.00
inventory 1g
10-20 days ฿14,571.00

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tert-butyl N-(5-bromothiophen-2-yl)carbamate
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This chemical is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. It is often employed in the construction of thiophene-based compounds, which are significant in the pharmaceutical and agrochemical industries. The presence of the bromine atom makes it a valuable building block for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. Additionally, the tert-butyl carbamate group serves as a protec

This chemical is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. It is often employed in the construction of thiophene-based compounds, which are significant in the pharmaceutical and agrochemical industries. The presence of the bromine atom makes it a valuable building block for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. Additionally, the tert-butyl carbamate group serves as a protective group for amines, allowing selective reactions to occur at other sites of the molecule. This compound is particularly useful in the synthesis of heterocyclic compounds, which are commonly found in drugs and biologically active molecules. Its applications extend to material science, where it can be used to create novel polymers or organic electronic materials.

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