(E)-tert-Butyl 4-bromo-3-(4-ethoxy-4-oxobut-2-en-1-yl)thiophene-2-carboxylate

95%

Reagent Code: #181091
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CAS Number 2828433-77-6

science Other reagents with same CAS 2828433-77-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 375.28 g/mol
Formula C₁₅H₁₉BrO₄S
thermostat Physical Properties
Boiling Point 442.0±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.347±0.06 g/cm3(Predicted)
Storage Room temperature, away from light, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex thiophene-based molecules. The presence of the α,β-unsaturated ester moiety makes it suitable for Michael addition reactions, useful in forming carbon-carbon bonds. It is also employed in the development of conjugated systems for materials science applications, including organic semiconductors and electronic materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,150.00
inventory 250mg
10-20 days ฿22,310.00

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(E)-tert-Butyl 4-bromo-3-(4-ethoxy-4-oxobut-2-en-1-yl)thiophene-2-carboxylate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex thiophene-based molecules. The presence of the α,β-unsaturated ester moiety makes it suitable for Michael addition reactions, useful in forming carbon-carbon bonds. It is also employed in the development of conjugated systems for materia

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex thiophene-based molecules. The presence of the α,β-unsaturated ester moiety makes it suitable for Michael addition reactions, useful in forming carbon-carbon bonds. It is also employed in the development of conjugated systems for materials science applications, including organic semiconductors and electronic materials.

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