Methyl 5-methyl-4-nitrothiophene-2-carboxylate
96%
- Product Code: 49159
CAS:
56921-01-8
| Molecular Weight: | 201.2000 g./mol | Molecular Formula: | C₇H₇NO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18642553 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. It is particularly valuable in the pharmaceutical industry, where it serves as a building block for the synthesis of various bioactive compounds. Its nitro and ester functional groups make it a versatile precursor in reactions such as nucleophilic substitutions and reductions, enabling the creation of diverse thiophene derivatives. These derivatives are often explored for their potential therapeutic applications, including antimicrobial, anti-inflammatory, and anticancer properties. Additionally, it finds use in material science for the development of organic electronic materials, where thiophene-based compounds are known for their conductive and optoelectronic properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $107.95 |
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Methyl 5-methyl-4-nitrothiophene-2-carboxylate
This chemical is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. It is particularly valuable in the pharmaceutical industry, where it serves as a building block for the synthesis of various bioactive compounds. Its nitro and ester functional groups make it a versatile precursor in reactions such as nucleophilic substitutions and reductions, enabling the creation of diverse thiophene derivatives. These derivatives are often explored for their potential therapeutic applications, including antimicrobial, anti-inflammatory, and anticancer properties. Additionally, it finds use in material science for the development of organic electronic materials, where thiophene-based compounds are known for their conductive and optoelectronic properties.
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