CAS 17667-32-2

Benzoic acid, 2-bromo-4,5-dimethoxy-, methyl ester

Description:

Benzoic acid, 2-bromo-4,5-dimethoxy-, methyl ester, with the CAS number 17667-32-2, is an organic compound characterized by its ester functional group and the presence of bromine and methoxy substituents on the aromatic ring. This compound typically appears as a white to off-white solid and is soluble in organic solvents such as ethanol and acetone, but has limited solubility in water due to its hydrophobic aromatic structure. The presence of the bromine atom introduces a halogen, which can influence the compound's reactivity and potential applications in organic synthesis. The methoxy groups contribute to the electron-donating properties of the molecule, which can affect its chemical behavior and interactions. Benzoic acid derivatives, including this compound, are often studied for their potential use in pharmaceuticals, agrochemicals, and as intermediates in organic synthesis. Safety data should be consulted for handling and storage, as with all chemical substances, to ensure proper precautions are taken.

Formula: C₁₀H₁₁BrO₄

InChI: InChI=1S/C10H11BrO4/c1-13-8-4-6(10(12)15-3)7(11)5-9(8)14-2/h4-5H,1-3H3

InChI key: InChIKey=BCUHOZBMHZWCGL-UHFFFAOYSA-N

SMILES: C(OC)(=O)C1=CC(OC)=C(OC)C=C1Br

Synonyms:

• Methyl 2-bromo-4,5-dimethoxybenzoate
• Methyl 6-bromoveratrate
• Benzoic acid, 2-bromo-4,5-dimethoxy-, methyl ester
• Veratric acid, 6-bromo-, methyl ester
• Methyl 6-bromo-3,4-dimethoxybenzoate

Benzoic acid, 2-bromo-4,5-dimethoxy-, methyl ester

CAS: 17667-32-2

Formula: C₁₀H₁₁BrO₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 275.0959

Ref: IN-DA0024TX

Methyl 2-bromo-4,5-dimethoxybenzoate

CAS: 17667-32-2

Methyl 2-bromo-4,5-dimethoxybenzoate

Purity: 98%

Molecular weight: 275.1g/mol

Ref: 54-OR1074196

Methyl 6-bromo-3,4-dimethoxybenzoate

CAS: 17667-32-2

Methyl 6-bromo-3,4-dimethoxybenzoate is a potent compound that inhibits topoisomerase. It is not as selective as other topoisomerase inhibitors, but it is more reactive and has been shown to be effective in the synthesis of lactones. This compound can also be used as an intermediate for the synthesis of more potent inhibitors of topoisomerase. Methyl 6-bromo-3,4-dimethoxybenzoate has been shown to react with aliphatic aldehydes and nitro compounds to form zinc powder. The reaction proceeds via a catalytic mechanism involving an initial complexation of the methyl group with the carbonyl oxygen atom followed by nucleophilic attack by zinc.

Formula: C₁₀H₁₁BrO₄

Purity: Min. 98 Area-%

Color and Shape: Powder

Molecular weight: 275.1 g/mol

Ref: 3D-FB70592

Methyl-2-bromo-4,5-dimethoxybenzoate

CAS: 17667-32-2

Formula: C₁₀H₁₁BrO₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 275.098

Ref: 10-F035101