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| 4-Bromoveratrole Basic information |
| 4-Bromoveratrole Chemical Properties |
| Hazard Codes | Xi | | Safety Statements | 23-24/25 | | WGK Germany | 3 | | TSCA | T | | HS Code | 29093038 |
| 4-Bromoveratrole Usage And Synthesis |
| Chemical Properties | Colorless to Yellow liquid | | Uses | 4-Bromoveratrole is a metabolite of bromobenzene, with a catechol moiety in the substructure. It also has use as a redox shuttle additive, essentially a component in lithium batteries that consumes excess current during overcharge. It is also used in the synthesis of the isoquinoline alkaloid (-)-mesembrine. | | Biological Functions | 4-Bromoveratrole has been shown that this molecule binds to the receptor for acetylcholine, which is found in the central nervous system and on muscles. The binding of 4-bromoveratrole to this receptor leads to the release of chloride ions from the cell, which increases the activity of acetylcholine. The detection sensitivity of 4-bromoveratrole in solution was determined by adding malonic acid or hydrochloric acid, which led to an increase in fluorescence intensity. This molecule also has fatty acid and hydroxyl groups that have been shown to have anti-inflammatory properties. |
| 4-Bromoveratrole Preparation Products And Raw materials |
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