CAS 5000-65-7
:2-Bromo-3′-methoxyacetophenone
Description:
2-Bromo-3′-methoxyacetophenone, with the CAS number 5000-65-7, is an organic compound that belongs to the class of acetophenones. It features a bromine atom and a methoxy group attached to the aromatic ring, which influences its chemical reactivity and physical properties. This compound typically appears as a solid at room temperature and is characterized by its moderate solubility in organic solvents such as ethanol and dichloromethane, while being less soluble in water due to its hydrophobic nature. The presence of the bromine atom enhances its electrophilic character, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions. The methoxy group can also participate in electron-donating effects, which can stabilize certain intermediates during chemical transformations. 2-Bromo-3′-methoxyacetophenone is often utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its versatile reactivity and the ability to serve as a building block for more complex molecules. Safety precautions should be observed when handling this compound, as it may pose health risks.
Formula:C9H9BrO2
InChI:InChI=1/C9H9BrO2/c1-12-8-4-2-3-7(5-8)9(11)6-10/h2-5H,6H2,1H3
InChI key:InChIKey=IOOHBIFQNQQUFI-UHFFFAOYSA-N
SMILES:C(CBr)(=O)C1=CC(OC)=CC=C1
Synonyms:- 2-Bromo-1-(3-Methoxyphenyl)Ethanone
- 2-Bromo-1-(3-methoxyphenyl)ethan-1-one
- 2-Bromo-1-(3-methoxyphenyl-1-yl)ethanone
- 2-Bromo-1-[3-(methyloxy)phenyl]ethanone
- 2-Bromo-3-methoxyacotophenone
- 2-Bromo-m-methoxyacetophenone
- 3-Methoxyphenacyl bromide
- Acetophenone, 2-bromo-3′-methoxy-
- Bromomethyl 3-Methoxyphenyl Ketone
- Ethanone, 2-bromo-1-(3-methoxyphenyl)-
- NSC 405833
- alpha-Bromo-3-methoxyacetophenone
- m-(Bromoacetyl)anisole
- m-Methoxyphenacyl bromide
- α-Bromo-3′-methoxyacetophenone
- α-Bromo-m-methoxyacetophenone
- ω-Bromo-3-methoxyacetophenone
- 2-BROMO-3''-METHOXYACETOPHENONE 97%
- 2-BROMO-3'-METHOXYACETOPHENONE
- AKOS BBS-00003869
- 3'-Methoxyphenacyl Bromide [for HPLC Labeling]
- 1-(Bromoacetyl)-3-methoxybenzene
- ALPHA-BROMO-M-METHOXYACETOPHENONE
- See more synonyms
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Found 9 products.
3'-Methoxyphenacyl Bromide
CAS:Formula:C9H9BrO2Purity:>98.0%(GC)(T)Color and Shape:White to Almost white powder to crystalMolecular weight:229.073'-Methoxyphenacyl Bromide [for HPLC Labeling]
CAS:Formula:C9H9BrO2Purity:>99.0%(GC)(T)Color and Shape:White to Almost white powder to crystalMolecular weight:229.072-Bromo-3'-methoxyacetophenone, 98%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C9H9BrO2Purity:98%Color and Shape:Crystals or powder or crystalline powder, Pale creamMolecular weight:229.072-Bromo-1-(3-Methoxyphenyl)Ethanone
CAS:Formula:C9H9BrO2Purity:98%Color and Shape:SolidMolecular weight:229.07063-Methoxyphenacyl bromide
CAS:3-Methoxyphenacyl bromideFormula:C9H9BrO2Purity:97%Color and Shape: yellow solidMolecular weight:229.07g/mol2-Bromo-3'-methoxyacetophenone
CAS:Controlled Product<p>Applications Derivatizing reagent.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Webster, S., et al.: Bioorg. Med. Chem. Lett., 20, 3265 (2010), Chezal, J., et al.: Eur. J. Med. Chem., 45, 2044 (2010),<br></p>Formula:C9H9BrO2Color and Shape:NeatMolecular weight:229.072-Bromo-3'-methoxyacetophenone
CAS:<p>2-Bromo-3'-methoxyacetophenone is a reactive compound that has been used as an antiplatelet drug. It is a prodrug of vicagrel, which inhibits the platelet aggregation by blocking the conversion of ADP to ATP. It also has been shown to inhibit the growth of cryptococcus neoformans. This compound binds to matrix proteins and disrupts their structure, leading to a decrease in platelet adhesion. 2-Bromo-3'-methoxyacetophenone has been shown to be metabolized through a number of metabolic transformations, including hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid. The biological properties of this drug are complex and depend on its concentration and duration of exposure. Its effect on platelet aggregation is due to its ability to inhibit the activity of protein kin</p>Formula:C9H9BrO2Purity:Min. 95%Molecular weight:229.07 g/mol3-Methoxyphenacyl bromide
CAS:Formula:C9H9BrO2Purity:98%Color and Shape:SolidMolecular weight:229.073







