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| 3,5-Dimethoxytoluene Basic information |
| Product Name: | 3,5-Dimethoxytoluene | | Synonyms: | 3,5-DIMETHOXYTOLUENE;3,5-DiMethoxytoluene, GC 98%;ORCINOL DIMETHYL ETHER;3,5-Dimethoxy-1-methylbenzene;5-Methylresorcinol dimethyl ether;Benzene, 1,3-dimethoxy-5-methyl-;Toluene, 3,5-dimethoxy-;1,5-Dimethoxy-3-methylbenzene | | CAS: | 4179-19-5 | | MF: | C9H12O2 | | MW: | 152.19 | | EINECS: | 224-048-9 | | Product Categories: | Building Blocks;C9;Aromatic Ethers;Ethers;Organic Building Blocks;Oxygen Compounds;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds | | Mol File: | 4179-19-5.mol |
| 3,5-Dimethoxytoluene Chemical Properties |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 3 | | TSCA | Yes | | HS Code | 29093090 |
| 3,5-Dimethoxytoluene Usage And Synthesis |
| Chemical Properties | Clear colorless to yellow liquid | | Uses | 3,5-Dimethoxytoluene (DMT) may be used in the synthesis of 3,5-dimethoxybenzoic acid by oxidation and 2-methoxy-6-methyl-1,4-benzoquinone by catalytic oxidation with hydrogen peroxide (H2O2)/methyltrioxorhenium (CH3ReO3) in dimethyl carbonate (DMC). | | Synthesis Reference(s) | Organic Syntheses, Coll. Vol. 6, p. 859, 1988The Journal of Organic Chemistry, 70, p. 3275, 2005 DOI: 10.1021/jo050075r | | General Description | 3,5-Dimethoxytoluene (DMT) is a methoxylated phenolic derivative. It is reported to be one of the main constituent of the floral volatiles in different rose varieties. It has been biosynthesized from orcinol by two successive methylation catalyzed by O-methyltransferases (OMTs). The features of its aerobic oxidation with metal/bromide catalysts have been investigated. |
| 3,5-Dimethoxytoluene Preparation Products And Raw materials |
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