CAS 2314-36-5

3,5-Dichloro-4-hydroxybenzaldehyde

Description:

3,5-Dichloro-4-hydroxybenzaldehyde, with the CAS number 2314-36-5, is an organic compound that belongs to the class of chlorinated phenolic aldehydes. It features a benzene ring substituted with two chlorine atoms at the 3 and 5 positions, a hydroxyl group (-OH) at the 4 position, and an aldehyde group (-CHO) at the 1 position. This compound is typically a solid at room temperature and is characterized by its pale yellow to off-white crystalline appearance. It 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 both electron-withdrawing chlorine atoms and the electron-donating hydroxyl group influences its reactivity, making it a useful intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Additionally, it exhibits potential biological activity, which may include antimicrobial or antifungal properties, although specific applications may vary based on further research and development.

Formula: C₇H₄Cl₂O₂

InChI: InChI=1/C7H4Cl2O2/c8-5-1-4(3-10)2-6(9)7(5)11/h1-3,11H

SMILES: c1c(cc(c(c1Cl)O)Cl)C=O

Benzaldehyde, 3,5-dichloro-4-hydroxy-

CAS: 2314-36-5

Formula: C₇H₄Cl₂O₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 191.0115

Ref: IN-DA002MBJ

3,5-Dichloro-4-hydroxybenzaldehyde

CAS: 2314-36-5

3,5-Dichloro-4-hydroxybenzaldehyde

Formula: C₇H₄Cl₂O₂

Purity: ≥95%

Color and Shape: white solid

Molecular weight: 191.01g/mol

Ref: 54-OR27469

3,5-Dichloro-4-hydroxybenzaldehyde

CAS: 2314-36-5

3,5-Dichloro-4-hydroxybenzaldehyde is a triiodomethane derivative that reacts with chlorine to form a chlorinated aldehyde. It is used as an intermediate in the production of 4-hydroxybenzoic acid from phenylacetic acid and 4,4'-dichlorodiphenyl sulfone. 3,5-Dichloro-4-hydroxybenzaldehyde can be decarboxylated at elevated temperatures to produce formic acid. This compound has been used in wastewater treatment as it can remove chlorine byproducts and other pollutants such as nitrates, nitrites, and iron ions. The reaction kinetics of 3,5-dichloro-4-hydroxybenzaldehyde have been studied using hydroxymethyl groups and formyl groups to determine the rate of demethylation. The rates were found to be dependent on temperature.

Formula: C₇H₄Cl₂O₂

Purity: Min. 95%

Color and Shape: White Powder

Molecular weight: 191.01 g/mol

Ref: 3D-FD70957

3,5-Dichloro-4-hydroxybenzaldehyde

CAS: 2314-36-5

Formula: C₇H₄Cl₂O₂

Purity: 95%

Color and Shape: Solid, White to off-white powder

Molecular weight: 191.01

Ref: 10-F065155