10504-04-8

Usage

Uses

Used in Chemical Synthesis:
2,3,5-Trimethylfuran is used as a solvent in chemical reactions for its ability to dissolve a wide range of substances, facilitating various chemical processes.
Used in Chemical Production:
It serves as an intermediate in the production of other chemicals, contributing to the synthesis of complex organic compounds.
Used in Biofuel Industry:
2,3,5-Trimethylfuran is used as a potential biofuel due to its high energy content and the reduced environmental impact compared to traditional fossil fuels, offering a sustainable energy alternative.
Used in Flavor and Fragrance Industry:
It is utilized as a flavor and fragrance ingredient, capitalizing on its sweet odor to enhance the sensory properties of various products.
Used in Antimicrobial Applications:
2,3,5-Trimethylfuran is explored for its antimicrobial properties, indicating potential use in sanitizing products or as a preservative in different industries to inhibit microbial growth.

InChI:InChI=1/C7H10O/c1-5-4-6(2)8-7(5)3/h4H,1-3H3

Upstream product

• 28730-32-7 2,4,5-trimethylfuran-3-carboxylic acid 
• 855906-54-6 3,4,6-trimethyl-[1,2]oxathiin-2,2-dioxide 
• 52480-43-0 4,5-dimethyl-2-formylfuran 
• 62664-62-4 ethyl 2,4,5-trimethylfuran-3-carboxylate 
• 857821-95-5 (3-ethoxycarbonyl-4,5-dimethyl-[2]furyl)-acetic acid ethyl ester 
• 53670-70-5 2-acetyl-3-methyl-4-oxopentanoic acid ethyl ester 
• 857821-97-7 (3-carboxy-4,5-dimethyl-[2]furyl)-acetic acid 

Downstream Products

• 97204-34-7 (Z)-3-Methyl-hex-3-ene-2,5-dione 
• 1795-05-7 2,4,5-trimethylthiophene 
• 97204-35-8 Acetic acid (Z)-2-methyl-3-oxo-but-1-enyl ester 

Relevant academic research and scientific papers

1H and 13C NMR Spectra of Some 2-Substituted 4,5-Dimethylfurans

1H and 13C NMR spectra of 22 2-substituted 4,5-dimethylfurans are reported.The J(C,H) values were used for signal assignments and for the identification of geometrical isomers of some derivatives. KEY WORDS: 2-Substituted 4,5-dimethylfurans, 1H and 13C NMR spectra

METAL CATALYST AND HYDROGEN GAS FREE APPROACHES FOR SELECTIVE REDUCTION OF ALDEHYDE TO METHYL GROUP OF DIFFERENT SUBSTITUTED FURANS

The present invention relates to 5-methyl substituted furan compounds of general formula (I) and process for the preparation thereof: OR1R2 R3CH3(I) Particularly, the present invention relates to a metal catalyst and hydrogen gas free, atom-economy, highly selective and low-cost process for the preparation of methyl substituted furan compounds from different aldehyde substituted furan compounds.

Hydrogen peroxide oxidation of polysubstituted pyrylium salts: Formation of enol esters and furans

2,4,6-Trialkylsubstituted pyrylium salts 1 have been known to afford 2-acyl-3,5-dialkyl-furans 2 in moderate yields (30 - 45%). Oxidation of these salts in buffer solutions (pH = 3-4.5) increased the yields of acylfurans to 75%. In contrast, tetra- and pe