620-02-0
Chemical Structure
5-Methylfurfural
- CAS No.: 620-02-0
- Formula:C6H6O2
- Molecular Weight:110.11
IUPAC Name: 5-methylfuran-2-carbaldehyde
InChIKey: OUDFNZMQXZILJD-UHFFFAOYSA-N
SMILES: O=CC1=CC=C(C)O1
Biological Activity: 5-Methylfurfural is a chemical that can be utilized as food additive, intermediate in the production of agrochemicals, and precursor of certain anti-cancer natural products. 5-Methylfurfural is formed during the photoexposition of ranitidine hydrochloride. 5-Methylfurfural is an organic compound. 5-Methylfurfural has a strong tendency to be further hydrogenated to 2,5-dimethylfuran (DMF). 5-Methylfurfural can predominantly evoke skin inflammation and barrier disintegration. 5-Methylfurfural degrades native DNA through the formation of single-strand breaks[1][2][3][4][5].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
5-Methylfurfural | 99.98% | 5-Methylfurfural is a chemical that can be utilized as food additive, intermediate in the production of agrochemicals, and precursor of certain anti-cancer natural products. 5-Methylfurfural is formed during the photoexposition of ranitidine hydrochloride. 5-Methylfurfural is an organic compound. 5-Methylfurfural has a strong tendency to be further hydrogenated to 2,5-dimethylfuran (DMF). 5-Methylfurfural can predominantly evoke skin inflammation and barrier disintegration. 5-Methylfurfural degrades native DNA through the formation of single-strand breaks. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
5-Methylfurfural (Standard) | ≥98% | 5-Methylfurfural (Standard) is the analytical standard of 5-Methylfurfural. This product is intended for research and analytical applications. 5-Methylfurfural is a chemical that can be utilized as food additive, intermediate in the production of agrochemicals, and precursor of certain anti-cancer natural products. 5-Methylfurfural is formed during the photoexposition of ranitidine hydrochloride. 5-Methylfurfural is an organic compound. 5-Methylfurfural has a strong tendency to be further hydrogenated to 2,5-dimethylfuran (DMF). 5-Methylfurfural can predominantly evoke skin inflammation and barrier disintegration. 5-Methylfurfural degrades native DNA through the formation of single-strand breaks. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. Lin Dong, et al., Selective hydrogenolysis of 5-hydroxymethylfurfural to 5-methylfurfural over Au/TiO2, Applied Catalysis B: Environmental, Volume 335, 2023, 122893, ISSN 0926-3373.
- [2]. Marzena Jamrógiewicz, et al., Detection of some volatile degradation products released during photoexposition of ranitidine in a solid state, Journal of Pharmaceutical and Biomedical Analysis, Volume 76, 2013, Pages 177-182, ISSN 0731-7085.
- [3]. Li, S., et al., (2021). Selective hydrogenation of 5-(hydroxymethyl)furfural to 5-methylfurfural over single atomic metals anchored on Nb2O5. Nature communications, 12(1), 584. [Content Brief]
- [4]. Lin, Y. K., et al., (2024). Systematic establishment of the relationship between skin absorption and toxicity of furanoids via in silico, in vitro, and in vivo assessments. Environmental research, 261, 119757. [Content Brief]
- [5]. Shahabuddin, Rahman, A., & Hadi, S. M. (1990). Specificity of the in vitro interaction of methylfurfural with DNA. Mutagenesis, 5(2), 131–136. [Content Brief]
