2-Acetyl-5-bromothiophene

99%

Reagent Code: #134516
label
Alias 2-acetyl-5-bromothiophene; 2-acetyl-5-bromothiophene
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CAS Number 5370-25-2

science Other reagents with same CAS 5370-25-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.07 g/mol
Formula C₆H₅BrOS
badge Registry Numbers
EC Number 226-363-7
MDL Number MFCD00014528
thermostat Physical Properties
Melting Point 94-96 °C(lit.)
Boiling Point 103 °C/4 mm Hg(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules due to the presence of both acetyl and bromo functional groups. The bromine atom allows for further cross-coupling reactions, making it valuable in building complex organic structures. Commonly employed in the preparation of thiophene-based derivatives with potential antimicrobial, anti-inflammatory, or antitumor activities. Also utilized in material science for designing organic semiconductors and conjugated polymers.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿180.00
5g
10-20 days ฿480.00
25g
10-20 days ฿1,490.00
100g
10-20 days ฿4,880.00
500g
10-20 days ฿24,100.00
2-Acetyl-5-bromothiophene
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules due to the presence of both acetyl and bromo functional groups. The bromine atom allows for further cross-coupling reactions, making it valuable in building complex organic structures. Commonly employed in the preparation of thiophene-based derivatives with potential antimicrobial, anti-inflammatory, or antitumor activities. Also utilized in material science for designing org
Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules due to the presence of both acetyl and bromo functional groups. The bromine atom allows for further cross-coupling reactions, making it valuable in building complex organic structures. Commonly employed in the preparation of thiophene-based derivatives with potential antimicrobial, anti-inflammatory, or antitumor activities. Also utilized in material science for designing organic semiconductors and conjugated polymers.
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