2,3,5-Tribromo-4-methylthiophene

≥95%

Reagent Code: #240255
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CAS Number 67869-13-0

science Other reagents with same CAS 67869-13-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 334.85 g/mol
Formula C₅H₃Br₃S
badge Registry Numbers
MDL Number MFCD00130086
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound serves as a building block in heterocyclic chemistry due to the presence of multiple bromine atoms and a thiophene ring. The bromine substituents allow for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex organic molecules. It is also employed in the development of organic semiconductors and electronic materials, where brominated thiophene derivatives help tune electronic properties and improve material stability. Additionally, it finds use in research settings for the preparation of ligands and catalysts in transition metal-mediated transformations.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,010.00
inventory 25g
10-20 days ฿4,630.00
2,3,5-Tribromo-4-methylthiophene
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound serves as a building block in heterocyclic chemistry due to the presence of multiple bromine atoms and a thiophene ring. The bromine substituents allow for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex organic molecules. It is also employed in the development of organic semiconductors and electronic materials, where brominat

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound serves as a building block in heterocyclic chemistry due to the presence of multiple bromine atoms and a thiophene ring. The bromine substituents allow for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex organic molecules. It is also employed in the development of organic semiconductors and electronic materials, where brominated thiophene derivatives help tune electronic properties and improve material stability. Additionally, it finds use in research settings for the preparation of ligands and catalysts in transition metal-mediated transformations.

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