| CAS ID | 4282-32-0 |
|---|---|
| IUPAC Name | 5 dicarboxylate, Dimethyl furan 2 |
| Molecular Formula | C8H8O5 |
| Molecular Weight | |
| SMILES | COC(=O)C1=CC=C(O1)C(=O)OC |
| CAS ID | 4282-32-0 |
|---|---|
| IUPAC Name | 5 dicarboxylate, Dimethyl furan 2 |
| Molecular Formula | C8H8O5 |
| Molecular Weight | |
| SMILES | COC(=O)C1=CC=C(O1)C(=O)OC |
Dimethyl Furan 2,5 Dicarboxylate DMFD is as a starting material in producing polyester resins, which are used to manufacture fibers, films, and coatings. It is also a useful monomer in the production of biodegradable polymers.
Dimethyl Furan 2,5 Dicarboxylate (DMFD) is also a critical building block in synthesising various pharmaceuticals and agrochemicals. It is a starting material in producing several drug candidates, including antifungal and antitumor agents.
In addition, DMFD is used to produce speciality chemicals, including flavours and fragrances. It is also a precursor to various esters, which contribute to the aroma and taste of many foods and beverages.
Dimethyl Furan 2,5 Dicarboxylate DMFD is a safe and reliable chemical with low toxicity and high stability. It is widely used in laboratory research for the synthesis of novel compounds.
In conclusion, Dimethyl furan 2,5 dicarboxylate (DMFD) is a versatile chemical with numerous industrial applications. Its ability to serve as a starting material in producing polyester resins, pharmaceuticals, agrochemicals, and specialty chemicals makes it an essential component in many manufacturing processes. Low toxicity and high stability make it a safe and reliable choice for laboratory research.
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The dimethyl furan structure consists of two methyl groups bonded to the aromatic ring of the furan chemical, which increases its stability and changes its reactivity compared to unsubstituted furan.
The dimethyl furan structure impacts its solubility and boiling point, making it an ideal intermediate in complicated processes, especially when the furan chemical's distinctive features are sought.
Starting with the chemical formula for furan (C4H4O), dimethyl furan is formed by substituting two hydrogen atoms with methyl groups, resulting in a C6H8O formula and a unique molecular configuration.
Dimethyl furan is distinct due to its modified aromatic ring and increased electron density. These characteristics distinguish it from the more straightforward molecular formula for furan and broaden its industrial possibilities.
Its structure enables a high energy density and low water solubility, which make this modified furan chemical an effective and sustainable biofuel manufacturing option.
