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5832-01-9

Methyl 5-nitrothiophene-2-carboxylate

Catalog#: AR0035X5  |   CAS#: 5832-01-9  |   MDL#: MFCD02702303  |   MF: C6H5NO4S  |   MW: 187.1732

Packsize Purity Price Availability Quantity
1g 95% $6.00 Global Stock Buy Now Add To Cart
5g 95% $16.00 Global Stock Buy Now Add To Cart
100g 95% $231.00 Global Stock Buy Now Add To Cart
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Catalog Number AR0035X5
Chemical Name Methyl 5-nitrothiophene-2-carboxylate
CAS Number 5832-01-9
Molecular Formula C6H5NO4S
Molecular Weight 187.1732
MDL Number MFCD02702303
SMILES [O-][N+](=O)c1ccc(s1)C(=O)OC

Methyl 5-nitrothiophene-2-carboxylate is a versatile compound commonly employed in chemical synthesis as a key building block for the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and reactivity make it a valuable intermediate in organic synthesis, particularly in the creation of heterocyclic compounds.Due to its nitro and ester functionalities, Methyl 5-nitrothiophene-2-carboxylate can undergo a variety of reactions such as reduction, substitution, and cyclization, leading to the formation of diverse molecular structures. This compound is often utilized in the development of new compounds with potential biological activities or industrial applications.One significant application of Methyl 5-nitrothiophene-2-carboxylate is in the synthesis of thiophene-containing compounds, which are prevalent in medicinal chemistry and materials science. By incorporating this building block into the molecular structure, researchers can modify the properties of the final product, enhancing its bioavailability, stability, or reactivity.Furthermore, Methyl 5-nitrothiophene-2-carboxylate serves as a precursor for the preparation of sulfur-containing heterocycles, which are essential components in the design of pharmaceuticals with diverse therapeutic effects. Its ability to introduce both electron-withdrawing and electron-donating groups makes it a valuable tool for fine-tuning the chemical and biological properties of the target molecules.In conclusion, the strategic use of Methyl 5-nitrothiophene-2-carboxylate in chemical synthesis enables chemists to access a wide array of functionalized heterocyclic compounds with promising applications in drug discovery, material science, and beyond.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H302-H315-H319-H332-H335
Precautionary Statements P261-P280-P305+P351+P338
Class N/A
Packing Group N/A

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