Thiophene-3-carbonyl chloride

97%

Reagent Code: #242473
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CAS Number 41507-35-1

science Other reagents with same CAS 41507-35-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 146.59 g/mol
Formula C₆H₃ClOS
badge Registry Numbers
MDL Number MFCD00130090
thermostat Physical Properties
Melting Point 51-54 °C(lit.)
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. It reacts with amines to form amide bonds and with alcohols to form ester bonds, making it valuable in constructing bioactive molecules and other complex structures. Commonly employed in the preparation of thiophene-based derivatives that exhibit antimicrobial, anti-inflammatory, or antitumor activities. Also utilized in the synthesis of conjugated polymers and organic semiconductors due to the electron-rich nature of the thiophene ring, enhancing charge transport properties in electronic devices. Its reactivity allows for easy incorporation into larger molecular frameworks, facilitating drug discovery and materials science research.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,430.00
inventory 5g
10-20 days ฿15,720.00

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Thiophene-3-carbonyl chloride
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Used primarily as an intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. It reacts with amines to form amide bonds and with alcohols to form ester bonds, making it valuable in constructing bioactive molecules and other complex structures. Commonly employed in the preparation of thiophene-based derivatives that exhibit antimicrobial, anti-inflammatory, or antitumor activities. Also utilized in the synthesis of conjugated polymers and organic semiconductors du

Used primarily as an intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. It reacts with amines to form amide bonds and with alcohols to form ester bonds, making it valuable in constructing bioactive molecules and other complex structures. Commonly employed in the preparation of thiophene-based derivatives that exhibit antimicrobial, anti-inflammatory, or antitumor activities. Also utilized in the synthesis of conjugated polymers and organic semiconductors due to the electron-rich nature of the thiophene ring, enhancing charge transport properties in electronic devices. Its reactivity allows for easy incorporation into larger molecular frameworks, facilitating drug discovery and materials science research.

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