CAS 16414-34-9

5-Bromo-3,4-dihydroxybenzaldehyde

Description:

5-Bromo-3,4-dihydroxybenzaldehyde is an organic compound characterized by the presence of a bromine atom and two hydroxyl groups on a benzene ring, along with an aldehyde functional group. Its molecular structure features a bromobenzene core, where the bromine is positioned at the 5th carbon, while the hydroxyl groups are located at the 3rd and 4th positions, contributing to its dihydroxy nature. This compound is typically a solid at room temperature and may exhibit a pale yellow to brown color. It is soluble in organic solvents and has limited solubility in water due to its hydrophobic aromatic ring. The presence of hydroxyl groups enhances its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, the aldehyde group can participate in condensation reactions, further expanding its utility in organic synthesis. Its bromine substituent can also serve as a site for further functionalization, making 5-Bromo-3,4-dihydroxybenzaldehyde a versatile intermediate in the synthesis of more complex organic molecules.

Formula: C₇H₅BrO₃

InChI: InChI=1S/C7H5BrO3/c8-5-1-4(3-9)2-6(10)7(5)11/h1-3,10-11H

InChI key: InChIKey=GVSGSHGXUXLQNS-UHFFFAOYSA-N

SMILES: C(=O)C1=CC(Br)=C(O)C(O)=C1

Synonyms:

• 3,4-Dihydroxy-5-bromobenzaldehyde
• 3-Bromo-4,5-dihydroxybenzaldehyde
• 5-Bromo-3,4-dihydroxybenzaldehyde
• Benzaldehyde, 3-bromo-4,5-dihydroxy-
• Bromoprotocatechualdehyde
• NSC 139675
• Protocatechualdehyde, 5-bromo-
• 5-Bromoprotocatechualdehyde

Benzaldehyde, 3-bromo-4,5-dihydroxy-

CAS: 16414-34-9

Formula: C₇H₅BrO₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 217.0168

Ref: IN-DA001UOE

3-Bromo-4,5-dihydroxybenzaldehyde

CAS: 16414-34-9

3-Bromo-4,5-dihydroxybenzaldehyde

Purity: 95%

Molecular weight: 217.02g/mol

Ref: 54-OR76665

5-Bromo-3,4-dihydroxybenzaldehyde

CAS: 16414-34-9

5-Bromo-3,4-dihydroxybenzaldehyde (5BDBA) is a chemical compound that can be used as a reactive dye and photochemical crosslinker in the preparation of polymers. 5BDBA has been shown to have chemoattractant properties for immune cells, such as activated T lymphocytes and neutrophils. It also has been shown to have an effect on β-cells in the pancreas and skin cells. This compound has been found to activate the nuclear factor kappa-light-chain enhancer (NFκB), which leads to increased expression of chemoattractant protein (MCP). In 3T3-L1 preadipocytes, 5BDBA has been shown to induce accumulation of fatty acids by activating peroxisome proliferator activator receptor gamma.

Formula: C₇H₅BrO₃

Purity: Min. 95%

Color and Shape: Yellow Powder

Molecular weight: 217.02 g/mol

Ref: 3D-FB70549

3-Bromo-4,5-dihydroxybenzaldehyde

CAS: 16414-34-9

Purity: 95%

Color and Shape: Solid

Molecular weight: 217.0180054

Ref: 10-F612145