(E)-3-(5-Bromothiophen-2-yl)acrylic acid

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Reagent Code: #184604
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CAS Number 50868-68-3

science Other reagents with same CAS 50868-68-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.08 g/mol
Formula C₇H₅BrO₂S
badge Registry Numbers
MDL Number MFCD03002751
thermostat Physical Properties
Boiling Point 350.1±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.783±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof storage, inert atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active compounds. Its conjugated structure and reactive functional groups make it valuable in cross-coupling reactions, such as Suzuki and Heck reactions, enabling the construction of complex organic molecules. Commonly employed in the preparation of thiophene-based derivatives that exhibit antimicrobial, anti-inflammatory, or antitumor properties. Also utilized in materials science for designing organic semiconductors and conjugated polymers due to the electron-rich nature of the thiophene ring.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿750.00
inventory 1g
10-20 days ฿2,980.00
inventory 5g
10-20 days ฿12,830.00

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(E)-3-(5-Bromothiophen-2-yl)acrylic acid
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active compounds. Its conjugated structure and reactive functional groups make it valuable in cross-coupling reactions, such as Suzuki and Heck reactions, enabling the construction of complex organic molecules. Commonly employed in the preparation of thiophene-based derivatives that exhibit antimicrobial, anti-inflammatory, or antitumor properties. Also utilized in materials s

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active compounds. Its conjugated structure and reactive functional groups make it valuable in cross-coupling reactions, such as Suzuki and Heck reactions, enabling the construction of complex organic molecules. Commonly employed in the preparation of thiophene-based derivatives that exhibit antimicrobial, anti-inflammatory, or antitumor properties. Also utilized in materials science for designing organic semiconductors and conjugated polymers due to the electron-rich nature of the thiophene ring.

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