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Home  > Dimethyl 5-amino-3-methylthiophene-2,4-dicarboxylate

AD80074

103765-33-9 | Dimethyl 5-amino-3-methylthiophene-2,4-dicarboxylate

Packsize Purity Availability Price Discounted Price    Quantity
1g 99% in stock $42.00 $29.00 -   +
5g 99% in stock $136.00 $95.00 -   +
25g 99% in stock $409.00 $286.00 -   +
100g 99% in stock $1,356.00 $949.00 -   +
500g 99% in stock $4,385.00 $3,069.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AD80074
Chemical Name: Dimethyl 5-amino-3-methylthiophene-2,4-dicarboxylate
CAS Number: 103765-33-9
Molecular Formula: C9H11NO4S
Molecular Weight: 229.2529
MDL Number: MFCD00159553
SMILES: COC(=O)c1sc(c(c1C)C(=O)OC)N

 

Upstream Synthesis Route
  • Dimethyl 5-amino-3-methylthiophene-2,4-dicarboxylate is a versatile chemical compound widely used in chemical synthesis as a key building block for the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure containing both amino and ester functional groups makes it a valuable intermediate in organic synthesis.In chemical synthesis, Dimethyl 5-amino-3-methylthiophene-2,4-dicarboxylate can be utilized in the preparation of heterocyclic compounds, which are important components in many biologically active molecules. Its ability to undergo various chemical reactions such as nucleophilic substitution, esterification, and cyclization reactions allows for the efficient synthesis of complex molecules with diverse applications.Additionally, Dimethyl 5-amino-3-methylthiophene-2,4-dicarboxylate can act as a precursor for the synthesis of functionalized thiophene derivatives, which have emerged as valuable scaffolds in medicinal chemistry due to their potent biological activities. Its incorporation into drug molecules can impart desirable pharmacological properties, making it an essential building block for drug discovery and development processes.Overall, the strategic placement of Dimethyl 5-amino-3-methylthiophene-2,4-dicarboxylate in chemical synthesis plays a pivotal role in expanding the diversity of organic compounds available for various industrial applications, particularly in the pharmaceutical and agrochemical industries.
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