| Identification | More | [Name]
4-Bromoveratrole | [CAS]
2859-78-1 | [Synonyms]
1-BROMO-3,4-DIMETHOXYBENZENE
3,4-DIMETHOXYBROMOBENZENE
4-BROMO-1,2-DIMETHOXYBENZENE
4-BROMOCATECHOL DIMETHYL ETHER
4-BROMOVERATROLE
3,4-Dimethoxyphenyl bromide
4-bromo-1,2-dimethoxy-benzen
Bromoveratrole
p-Bromoveratrole
4-Bromo-1,2-dimethoxybenzene~3,4-Dimethoxybromobenzene
1-Bromo-3,4-dimetoxybenzene
4-Bromoveratrole98%
4-Brmomveratrole
1-BROMO-3,4-DIMETHOXYBENZENE/4-BROMOVERATROLE
4-Bromo-2-methoxyanisole
1,2-Dimethoxy-5-bromobenzene
3,4-Dimethoxy-1-bromobenzene
4-Bromoveratrol | [EINECS(EC#)]
220-677-8 | [Molecular Formula]
C8H9BrO2 | [MDL Number]
MFCD00008381 | [Molecular Weight]
217.06 | [MOL File]
2859-78-1.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Safety Statements ]
S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [TSCA ]
T | [HS Code ]
29093038 |
| Hazard Information | Back Directory | [Chemical Properties]
colorlesstolightyellowliqui | [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.
| [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.? |
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