CAS 6267-34-1
:2-Bromo-5-methoxy-1,3-dimethylbenzene
Description:
2-Bromo-5-methoxy-1,3-dimethylbenzene, also known by its CAS number 6267-34-1, is an organic compound belonging to the class of brominated aromatic hydrocarbons. Its molecular structure features a benzene ring substituted with a bromine atom, a methoxy group (-OCH3), and two methyl groups (-CH3) at specific positions, which contribute to its chemical properties and reactivity. This compound is typically characterized by its moderate polarity due to the presence of the methoxy group, which can influence its solubility in various solvents. The bromine substituent can enhance the compound's reactivity in electrophilic aromatic substitution reactions, making it useful in synthetic organic chemistry. Additionally, the presence of multiple substituents can affect the compound's physical properties, such as boiling and melting points, as well as its spectral characteristics in techniques like NMR and IR spectroscopy. Overall, 2-Bromo-5-methoxy-1,3-dimethylbenzene serves as a valuable intermediate in the synthesis of more complex organic molecules.
Formula:C9H11BrO
InChI:InChI=1S/C9H11BrO/c1-6-4-8(11-3)5-7(2)9(6)10/h4-5H,1-3H3
InChI key:InChIKey=RAWZVIWEDAGMPW-UHFFFAOYSA-N
SMILES:O(C)C1=CC(C)=C(Br)C(C)=C1
Synonyms:- 3,5-Dimethyl-4-bromoanisole
- 4-Bromo-1-methoxy-3,5-dimethylbenzene
- 4-Bromo-3,5-Dimethylanisole
- 4-Methoxy-2,6-dimethylbromobenzene
- Anisole, 4-bromo-3,5-dimethyl-
- Benzene, 2-bromo-5-methoxy-1,3-dimethyl-
- NSC 37991
- 2-Bromo-5-methoxy-1,3-dimethylbenzene
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Found 4 products.
2-Bromo-5-methoxy-1,3-dimethylbenzene
CAS:Formula:C9H11BrOPurity:97%Color and Shape:LiquidMolecular weight:215.08702-Bromo-5-methoxy-1,3-dimethylbenzene
CAS:2-Bromo-5-methoxy-1,3-dimethylbenzenePurity:98%Molecular weight:215.09g/mol4-Bromo-3,5-dimethylanisole
CAS:Formula:C9H11BrOPurity:97%Color and Shape:SolidMolecular weight:215.094-Bromo-3,5-dimethylbenzyl alcohol
CAS:<p>4-Bromo-3,5-dimethylbenzyl alcohol is a potent anticancer agent that is synthesized from bromoarenes. It has been shown to be effective against cancer cells in the presence of activated carbon, aluminum chloride, and organotellurium. 4-Bromo-3,5-dimethylbenzyl alcohol reacts with peptide hormones and other hormones at the cellular level by inhibiting DNA synthesis. This inhibition prevents the production of proteins that are vital for cell division. The reaction rate is rapid in solvents such as acetonitrile.>>END>></p>Formula:C9H11BrOPurity:Min. 95%Color and Shape:PowderMolecular weight:215.09 g/mol



