4-Bromothiophene-2-carbonyl chloride

95%

Reagent Code: #141228
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CAS Number 58777-65-4

science Other reagents with same CAS 58777-65-4

blur_circular Chemical Specifications

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Weight 225.49 g/mol
Formula C₅H₂BrClOS
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MDL Number MFCD04115391
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It serves as a building block for constructing more complex thiophene derivatives, which are valuable in the development of bioactive molecules. Its reactivity allows for easy introduction into larger conjugated systems, making it useful in the synthesis of organic semiconductors and electronic materials. Commonly employed in coupling reactions and acylation processes to form amides, esters, and ketones that are key in drug discovery and material science.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,990.00
inventory 1g
10-20 days ฿13,480.00
inventory 5g
10-20 days ฿47,150.00

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4-Bromothiophene-2-carbonyl chloride
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Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It serves as a building block for constructing more complex thiophene derivatives, which are valuable in the development of bioactive molecules. Its reactivity allows for easy introduction into larger conjugated systems, making it useful in the synthesis of organic semiconductors and electronic materials. Commonly employed in coupling reactions and acylation processes to form amides, esters,
Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It serves as a building block for constructing more complex thiophene derivatives, which are valuable in the development of bioactive molecules. Its reactivity allows for easy introduction into larger conjugated systems, making it useful in the synthesis of organic semiconductors and electronic materials. Commonly employed in coupling reactions and acylation processes to form amides, esters, and ketones that are key in drug discovery and material science.
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