CAS 61657-65-6
:3,5-dibromo-2-methoxybenzaldehyde
Description:
3,5-Dibromo-2-methoxybenzaldehyde is an organic compound characterized by its aromatic structure, featuring a benzaldehyde functional group along with two bromine substituents and a methoxy group. The presence of bromine atoms at the 3 and 5 positions of the benzene ring enhances the compound's reactivity and influences its physical properties, such as solubility and boiling point. The methoxy group at the 2 position contributes to the compound's electron-donating characteristics, which can affect its reactivity in electrophilic aromatic substitution reactions. This compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its applications can range from serving as an intermediate in organic synthesis to potential uses in pharmaceuticals or agrochemicals, depending on the specific reactivity and properties of the compound. Safety data should be consulted for handling, as halogenated compounds can pose environmental and health risks.
Formula:C8H6Br2O2
InChI:InChI=1/C8H6Br2O2/c1-12-8-5(4-11)2-6(9)3-7(8)10/h2-4H,1H3
SMILES:COc1c(cc(cc1Br)Br)C=O
Synonyms:- 3,5-Dibromosalicylaldehyde methyl ether
- 61657-65-6
- Vhr Ce Ee Bo1
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.
3,5-Dibromo-2-methoxybenzaldehyde
CAS:Formula:C8H6Br2O2Purity:97%Color and Shape:SolidMolecular weight:293.94003,5-Dibromo-2-methoxybenzaldehyde
CAS:3,5-Dibromo-2-methoxybenzaldehydePurity:96%Molecular weight:293.94004g/molRef: 10-F612847
1g38.00€5g75.00€10g103.00€1kg1,241.00€25g155.00€100g345.00€500g896.00€100mg20.00€250mg23.00€3,5-Dibromo-2-methoxybenzaldehyde
CAS:<p>3,5-Dibromo-2-methoxybenzaldehyde (3,5-DMB) is a x-ray crystal structure of a molecule. It is an organic compound that has the chemical formula of C10H8O4Br. 3,5-DMB is an intermediate in the synthesis of 6-methoxy-2-naphthol and has been crystallized from ethanolic solutions. 3,5-DMB can be efficiently synthesized by reacting malononitrile with piperidine in microwave irradiation. A reaction mechanism for this synthesis was proposed which involves the formation of a nitrile oxide intermediate followed by a one electron oxidation to form 3,5-DMB. This method can be used to generate high yields of 3,5-DMB in minutes and hours with good purity.</p>Formula:C8H6Br2O2Purity:Min. 95%Molecular weight:293.94 g/mol



