488-23-3
488-23-3
Chemical Structure
1,2,3,4-Tetramethylbenzene
- CAS No.: 488-23-3
- Formula:C10H14
- Molecular Weight:134.22
IUPAC Name: 1,2,3,4-tetramethylbenzene
InChIKey: UOHMMEJUHBCKEE-UHFFFAOYSA-N
SMILES: CC1=CC=C(C)C(C)=C1C
Biological Activity: 1,2,3,4-Tetramethylbenzene is an aromatic hydrocarbon. 1,2,3,4-Tetramethylbenzene can serve as a molecular marker indicating the input of photosynthetic sulfur bacteria (especially green sulfur bacteria) in ancient sedimentary environments, reflecting the static marine environment of the source rock deposition. 1,2,3,4-Tetramethylbenzene can also be used as a pharmaceutical intermediate[1][2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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1,2,3,4-Tetramethylbenzene | 98.00% | 1,2,3,4-Tetramethylbenzene is an aromatic hydrocarbon. 1,2,3,4-Tetramethylbenzene can serve as a molecular marker indicating the input of photosynthetic sulfur bacteria (especially green sulfur bacteria) in ancient sedimentary environments, reflecting the static marine environment of the source rock deposition. 1,2,3,4-Tetramethylbenzene can also be used as a pharmaceutical intermediate. | ||||||||||||||||||||
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1,2,3,4-Tetramethylbenzene (Standard) | ≥98% | 1,2,3,4-Tetramethylbenzene (Standard) is the analytical standard substance of 1,2,3,4-Tetramethylbenzene. This product is used for research and analytical applications. 1,2,3,4-Tetramethylbenzene is an aromatic hydrocarbon. 1,2,3,4-Tetramethylbenzene can serve as a molecular marker indicating the input of photosynthetic sulfur bacteria (especially green sulfur bacteria) in ancient sedimentary environments, reflecting the static marine environment of the source rock deposition. 1,2,3,4-Tetramethylbenzene can also be used as a drug intermediate. | ||||||||||||||||||||
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1,2,3,4-Tetramethylbenzene-d14 | 1,2,3,4-Tetramethylbenzene-d14 is the deuterium labeled 1,2,3,4-Tetramethylbenzene. | |||||||||||||||||||||
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2,3-Dimethylhydroquinone | 2,3-Dimethylhydroquinone (o-Xylohydroquinone) is a hydroquinone. 2,3-Dimethylhydroquinone can be oxidized by Myeloperoxidase. 2,3-Dimethylhydroquinone can be used in the research of inflammatory diseases. | |||||||||||||||||||||
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2,3,5-Trimethylphenol (Standard) | ≥98% | 2,3,5-Trimethylphenol is a phenolic compound. | ||||||||||||||||||||
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Trimethylhydroquinone (Standard) | ≥98% | Trimethylhydroquinone (Standard) is the analytical standard of Trimethylhydroquinone (HY-W017378). This product is intended for research and analytical applications. Trimethylhydroquinone is an active compound intermediate. Trimethylhydroquinone can condense with isophytol or phytol to produce synthetic Vitamin E (HY-B1278A). Trimethylhydroquinone serves as the parent compound for the synthesis of trimethylhydroquinone derivatives with antioxidant, anti-allergic, and 5-lipoxygenase inhibitory activities. | ||||||||||||||||||||
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2,4,6-Trimethylphenol (Standard) | ≥98% | 2,4,6-Trimethylphenol (Standard) is the analytical standard of 2,4,6-Trimethylphenol. This product is intended for research and analytical applications. 2,4,6-Trimethylphenol is a probe compound shown to react mainly with organic matter (3DOM*). 2,4,6-Trimethylphenol is rapidly oxidized by singlet oxygen in aqueous solution. | ||||||||||||||||||||
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2,3,6-Trimethylphenol | 2,3,6-Trimethylphenol (3-Hydroxypseudocumene) is an organic intermediate. The oxidation of 2,3,6-Trimethylphenol is the key step for the production of 2,3,5-trimethylbenzoquinone. | |||||||||||||||||||||
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3,4,5-Trimethylphenol | 3,4,5-Trimethylphenol is a phenolic compound. | |||||||||||||||||||||
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1,2,3,5-Tetramethylbenzene | 1,2,3,5-Tetramethylbenzene (Isodurene) is an aromatic hydrocarbon isomer of tetramethylbenzene. 1,2,3,5-Tetramethylbenzene serves as an important component of industrial organic solvents. 1,2,3,5-Tetramethylbenzene can be used in the organic synthesis of plastics and resins. 1,2,3,5-Tetramethylbenzene exhibits potential neurotoxicity, acute oral toxicity and mild skin irritation activity. | |||||||||||||||||||||
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References
- [1]. Ying Duan Lei, et al. Measuring the Octan-1-ol Air Partition Coefficient of Volatile Organic Chemicals with the Variable Phase Ratio Headspace Technique. Cite this: J. Chem. Eng. Data 2019, 64, 11, 4793–4800.
- [2]. Yoon Y W, et al. Spectroscopic Identification of Isomeric Trimethylbenzyl Radicals Generated from 1, 2, 3, 4-Tetramethylbenzene. Bulletin of the Korean Chemical Society, 2011, 32(8): 2751-2755.
- [3]. Wanglu J, et al. Source of 1, 2, 3, 4-tetramethylbenzene in asphaltenes from the Tarim Basin. Journal of Asian earth sciences, 2007, 30(5-6): 591-598.
- [4]. Kralj P, et al. Remarkable effect of water on functionalization of the phenyl ring in methyl-substituted benzene derivatives with F-TEDA-BF4. J Org Chem. 2006 May 12;71(10):3880-8. [Content Brief]
