634-36-6
Chemical Structure
1,2,3-Trimethoxybenzene
- CAS No.: 634-36-6
- Formula:C9H12O3
- Molecular Weight:168.19
IUPAC Name: 1,2,3-trimethoxybenzene
InChIKey: CRUILBNAQILVHZ-UHFFFAOYSA-N
SMILES: COC1=C(OC)C(OC)=CC=C1
Biological Activity: 1,2,3-Trimethoxybenzene is a model compound of lignin. 1,2,3-Trimethoxybenzene can potentially serve as a biomarker for certain foods due to its presence in tea. 1,2,3-Trimethoxybenzene can be used as a drug intermediate for synthesizing 2,6-dimethoxy-1,4-benzoquinone (HY-N1677)[1][2].
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1,2,3-Trimethoxybenzene | 99.81% | 1,2,3-Trimethoxybenzene is a model compound of lignin. 1,2,3-Trimethoxybenzene can potentially serve as a biomarker for certain foods due to its presence in tea. 1,2,3-Trimethoxybenzene can be used as a drug intermediate for synthesizing 2,6-dimethoxy-1,4-benzoquinone (HY-N1677). | ||||||||||||||||||||
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1,2,3-Trimethoxybenzene (Standard) | ≥98% | 1,2,3-Trimethoxybenzene (Standard) is an analytical standard for 1,2,3-Trimethoxybenzene (HY-W017092). This product is for research and analytical applications. 1,2,3-Trimethoxybenzene is a lignin model compound. Its presence in tea makes it a potential biomarker for certain foods. 1,2,3-Trimethoxybenzene can be used as a pharmaceutical intermediate in the synthesis of 2,6-dimethoxy-1,4-benzoquinone (HY-N1677). | ||||||||||||||||||||
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- [1]. Zheng Li, et al. Cleavage of ethers and demethylation of lignin in acidic concentrated lithium bromide (ACLB) solution.
- [2]. Bolker HI, Kung FL. Formation of 2, 6-dimethoxy-1, 4-benzoquinone by the action of nitrous acid of 1, 2, 3-trimethoxybenzene. Journal of the Chemical Society C: Organic. 1969(18):2298-304.