Methyl 4-bromo-3-methylthiophene-2-carboxylate
95%
- Product Code: 55621
CAS:
265652-38-8
Molecular Weight: | 235.10 g./mol | Molecular Formula: | C₇H₇BrO₂S |
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EC Number: | MDL Number: | MFCD14584476 | |
Melting Point: | Boiling Point: | 263.3±35.0 °C(Predicted) | |
Density: | 1.575±0.06 g/cm3(Predicted) | Storage Condition: | Store at room temperature, away from light, dry and sealed |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. It serves as a key intermediate in the production of pharmaceuticals, particularly in the synthesis of compounds with potential therapeutic properties. Its structure allows for further functionalization, making it valuable in the creation of thiophene derivatives, which are often explored for their biological activities. Additionally, it is employed in material science for the development of organic electronic materials, such as conductive polymers or semiconductors, due to the thiophene ring's electron-rich nature. Its application extends to agrochemical research, where it is used to design and synthesize novel compounds for crop protection.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿2,853.00 |
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0.250 | 10-20 days | ฿4,563.00 |
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1.000 | 10-20 days | ฿8,226.00 |
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Methyl 4-bromo-3-methylthiophene-2-carboxylate
This chemical is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. It serves as a key intermediate in the production of pharmaceuticals, particularly in the synthesis of compounds with potential therapeutic properties. Its structure allows for further functionalization, making it valuable in the creation of thiophene derivatives, which are often explored for their biological activities. Additionally, it is employed in material science for the development of organic electronic materials, such as conductive polymers or semiconductors, due to the thiophene ring's electron-rich nature. Its application extends to agrochemical research, where it is used to design and synthesize novel compounds for crop protection.
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