2-Thienylzinc bromide solution

0.5 M in THF

Reagent Code: #240045
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CAS Number 45438-80-0

science Other reagents with same CAS 45438-80-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.428 g/mol
Formula C₄H₃BrSZn
badge Registry Numbers
MDL Number MFCD01317002
thermostat Physical Properties
Boiling Point 66 °C
inventory_2 Storage & Handling
Density 0.973 g/mL at 25 °C
Storage 2-8°C

description Product Description

Widely used in organic synthesis, especially in cross-coupling reactions such as Negishi coupling, enabling the formation of carbon-carbon bonds between aromatic systems. It allows for the introduction of thiophene groups into complex molecules, which is valuable in the development of pharmaceuticals, agrochemicals, and organic electronic materials. The presence of the thiophene ring enhances electronic properties, making this reagent particularly useful in synthesizing conjugated polymers and small molecules for use in semiconductors, OLEDs, and solar cells. Its solution form facilitates handling and precise dosing in reaction setups.

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Size Availability Unit Price Quantity
inventory 50ml
10-20 days ฿18,950.00
2-Thienylzinc bromide solution
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Widely used in organic synthesis, especially in cross-coupling reactions such as Negishi coupling, enabling the formation of carbon-carbon bonds between aromatic systems. It allows for the introduction of thiophene groups into complex molecules, which is valuable in the development of pharmaceuticals, agrochemicals, and organic electronic materials. The presence of the thiophene ring enhances electronic properties, making this reagent particularly useful in synthesizing conjugated polymers and small mole

Widely used in organic synthesis, especially in cross-coupling reactions such as Negishi coupling, enabling the formation of carbon-carbon bonds between aromatic systems. It allows for the introduction of thiophene groups into complex molecules, which is valuable in the development of pharmaceuticals, agrochemicals, and organic electronic materials. The presence of the thiophene ring enhances electronic properties, making this reagent particularly useful in synthesizing conjugated polymers and small molecules for use in semiconductors, OLEDs, and solar cells. Its solution form facilitates handling and precise dosing in reaction setups.

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