611-13-2
611-13-2
Chemical Structure
Methyl 2-furoate
Synonym(s): Methyl furan-2-carboxylate
- No. CAS: 611-13-2
- Formula:C6H6O3
- Molecular Weight:126.11
IUPAC Name: methyl furan-2-carboxylate
InChIKey: HDJLSECJEQSPKW-UHFFFAOYSA-N
SMILES: O=C(C1=CC=CO1)OC
Biological Activity: Methyl 2-furoate (Methyl furan-2-carboxylate) is a furan ester and the methyl ester of Furan-2-carboxylic acid (HY-W012946). Methyl 2-furoate is found in the solid-state fermentation of Antrodia camphorata and is formed via the Maillard reaction between pea protein hydrolysates and fructose. Methyl 2-furoate serves as a synthetic intermediate in the synthesis of Furan-2-carbohydrazide[1][2][3][4][5].
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Methyl 2-furoate | 99.94% | Methyl 2-furoate (Methyl furan-2-carboxylate) is a furan ester and the methyl ester of Furan-2-carboxylic acid (HY-W012946). Methyl 2-furoate is found in the solid-state fermentation of Antrodia camphorata and is formed via the Maillard reaction between pea protein hydrolysates and fructose. Methyl 2-furoate serves as a synthetic intermediate in the synthesis of Furan-2-carbohydrazide. | ||||||||||||||||||||
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Methyl 2-furoate (Standard) | 99.95% | Methyl 2-furoate (Standard) (Methyl furan-2-carboxylate (Standard)) is the analytical standard of Methyl 2-furoate (HY-Y0949). This product is intended for research and analytical applications. Methyl 2-furoate (Methyl furan-2-carboxylate) is a furan ester and the methyl ester of Furan-2-carboxylic acid (HY-W012946). Methyl 2-furoate is found in the solid-state fermentation of Antrodia camphorata and is formed via the Maillard reaction between pea protein hydrolysates and fructose. Methyl 2-furoate serves as a synthetic intermediate in the synthesis of Furan-2-carbohydrazide. | ||||||||||||||||||||
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References
- [1]. Lee Y, et al. Volatile compounds formed by thermal reactions between mung bean, pea, and soybean enzyme-hydrolyzed proteins and reducing sugars[J]. 2026.
- [2]. Su H, et al. Design, synthesis and biological evaluation of novel compounds with conjugated structure as anti-tumor agents. Bioorg Med Chem. 2008 Sep 1;16(17):7992-8002. [Content Brief]
- [3]. Xia Y, et al. Changes in volatile compound composition of Antrodia camphorata during solid state fermentation. Journal of the science of food and agriculture. 2011 Oct;91(13):2463-70.
- [4]. Schmalzbauer M, et al. Redox-neutral photocatalytic C− H carboxylation of arenes and styrenes with CO2. Chem. 2020 Oct 8;6(10):2658-72.
- [5]. Patil M, et al. Fluorescence ‘turn-on’probe for nanomolar zn (II) detection in living cells and environmental samples[J]. New Journal of Chemistry, 2022, 46(28): 13774-13782.
