5-(3,4-Dichlorophenyl)thiophene-2-carboxylic acid
95%
- Product Code: 48167
CAS:
338793-86-5
| Molecular Weight: | 273.14 g./mol | Molecular Formula: | C₁₁H₆Cl₂O₂S |
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| EC Number: | MDL Number: | MFCD01316824 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive molecules, particularly those targeting specific enzymes or receptors. Its structure, featuring a thiophene ring and dichlorophenyl group, makes it valuable in designing compounds with potential therapeutic applications, such as anti-inflammatory, antimicrobial, or anticancer agents. Additionally, it is often employed in material science for the synthesis of organic semiconductors or conductive polymers due to its conjugated system, which can enhance electronic properties. Researchers also explore its use in agrochemicals for developing novel pesticides or herbicides, leveraging its chemical reactivity and structural features.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | £346.45 |
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| 1.000 | 10-20 days | £589.49 |
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5-(3,4-Dichlorophenyl)thiophene-2-carboxylic acid
This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive molecules, particularly those targeting specific enzymes or receptors. Its structure, featuring a thiophene ring and dichlorophenyl group, makes it valuable in designing compounds with potential therapeutic applications, such as anti-inflammatory, antimicrobial, or anticancer agents. Additionally, it is often employed in material science for the synthesis of organic semiconductors or conductive polymers due to its conjugated system, which can enhance electronic properties. Researchers also explore its use in agrochemicals for developing novel pesticides or herbicides, leveraging its chemical reactivity and structural features.
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