Methyl 5-methyl-4-nitrothiophene-2-carboxylate

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Reagent Code: #49159
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CAS Number 56921-01-8

science Other reagents with same CAS 56921-01-8

blur_circular Chemical Specifications

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Weight 201.2000 g/mol
Formula C₇H₇NO₄S
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MDL Number MFCD18642553
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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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inventory 100mg
10-20 days ฿2,745.00

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Methyl 5-methyl-4-nitrothiophene-2-carboxylate
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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 po

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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