2-(2-(5-bromothiophen-2-yl)ethoxy)ethan-1-ol

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Reagent Code: #141728
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CAS Number 2432029-09-7

science Other reagents with same CAS 2432029-09-7

blur_circular Chemical Specifications

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Weight 251.1407 g/mol
Formula C₈H₁₁BrO₂S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of conjugated polymers and small molecule semiconductors for organic electronics such as organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The bromothiophene moiety enables further functionalization via cross-coupling reactions like Suzuki or Stille coupling, allowing the construction of complex π-conjugated systems. The ethylene glycol side chain improves solubility in polar solvents and can influence film morphology in thin-film devices. Also explored in the synthesis of bioactive molecules due to the thiophene scaffold’s prevalence in pharmaceuticals.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,000.00
inventory 250mg
10-20 days ฿22,400.00
inventory 1g
10-20 days ฿44,800.00

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2-(2-(5-bromothiophen-2-yl)ethoxy)ethan-1-ol
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Used as an intermediate in organic synthesis, particularly in the development of conjugated polymers and small molecule semiconductors for organic electronics such as organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The bromothiophene moiety enables further functionalization via cross-coupling reactions like Suzuki or Stille coupling, allowing the construction of complex π-conjugated systems. The ethylene glycol side chain improves solubility in polar solvents and can influence

Used as an intermediate in organic synthesis, particularly in the development of conjugated polymers and small molecule semiconductors for organic electronics such as organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The bromothiophene moiety enables further functionalization via cross-coupling reactions like Suzuki or Stille coupling, allowing the construction of complex π-conjugated systems. The ethylene glycol side chain improves solubility in polar solvents and can influence film morphology in thin-film devices. Also explored in the synthesis of bioactive molecules due to the thiophene scaffold’s prevalence in pharmaceuticals.

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