ChemicalBook Product Catalog Chemical Reagents Organic reagents Aromatics 4-Bromoveratrole

4-Bromoveratrole

4-Bromoveratrole Basic information
Product Name:4-Bromoveratrole
Synonyms:1-BROMO-3,4-DIMETHOXYBENZENE / 4-BROMOVERATROLE;4-Bromoveratrole,97%;4-Bromoveratrole(4-bromo-1,2-dimethoxybenzene);4-Bromo-2-methoxyanisole;1,2-Dimethoxy-5-bromobenzene;3,4-Dimethoxy-1-bromobenzene;4-Bromoveratrol;Benzene, 4-broMo-1,2-diMethoxy-
CAS:2859-78-1
MF:C8H9BrO2
MW:217.06
EINECS:220-677-8
Product Categories:Anisole;Anisoles, Alkyloxy Compounds & Phenylacetates;Bromine Compounds;Aromatic Ethers
Mol File:2859-78-1.mol
4-Bromoveratrole Structure
4-Bromoveratrole Chemical Properties
Melting point 123 °C
Boiling point 255-256 °C (lit.)
density 1.509 g/mL at 25 °C (lit.)
refractive index n20/D 1.573(lit.)
Fp 229 °F
storage temp. Sealed in dry,Room Temperature
solubility Soluble in benzene, ether, toluene.
form Liquid
Specific Gravity1.702
color Clear colorless to slightly yellow
BRN 2046884
InChIKeyKBTMGSMZIKLAHN-UHFFFAOYSA-N
CAS DataBase Reference2859-78-1(CAS DataBase Reference)
NIST Chemistry ReferenceBenzene, 4-bromo-1,2-dimethoxy-(2859-78-1)
EPA Substance Registry SystemBenzene, 4-bromo-1,2-dimethoxy- (2859-78-1)
Safety Information
Hazard Codes Xi
Safety Statements 23-24/25
WGK Germany 3
TSCA T
HS Code 29093038
MSDS Information
ProviderLanguage
4-Bromo-1,2-dimethoxybenzene English
SigmaAldrich English
ACROS English
ALFA English
4-Bromoveratrole Usage And Synthesis
Chemical PropertiesColorless to Yellow liquid
Uses4-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 Functions4-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
Preparation Products4,5-Dimethoxy-1-cyanobenzocyclobutane-->1-BROMO-4,5-DIMETHOXY-2-NITROBENZENE-->3,4-Dimethoxyphenol-->4-Aminoveratrole-->(3,4-Dimethoxybicyclo[4.2.0]octa-1,3,5-trien-7-yl)methanamine hydrochloride-->1,2-DIMETHOXY-4-ETHYLBENZENE
2-BROMO-4,5-DIMETHOXYPHENYLACETIC ACID 2-Bromo-4,5-dimethoxyphenylacetonitrile 4-BROMOCATECHOL Bromoxynil Decabromodiphenyl Ethane 6-Bromoveratraldehyde Dimethoxybenzene 4,5-DIBROMOVERATROLE 1,2-Dimethoxybenzene 1-Bromo-3,4,5-trimethoxybenzene 4-Bromoveratrole 3-Bromoveratrole, 95% Phthalates Tetrabromobisphenol A bis(dibromopropyl ether) Benzyldodecyldimethylammonium bromide 4,4'-Bis(methoxymethyl)-1,1'-biphenyl 1,3-Dibromobenzene Decabromodiphenyl oxide
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