CAS 54373-15-8

4-(2-Chloroethoxy)benzaldehyde

Description:

4-(2-Chloroethoxy)benzaldehyde is an organic compound characterized by its aromatic structure, featuring a benzaldehyde functional group attached to a 2-chloroethoxy substituent. This compound typically appears as a colorless to pale yellow liquid with a distinct aromatic odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic aromatic ring. The presence of the chloroethoxy group introduces both polar and non-polar characteristics, influencing its reactivity and interactions in chemical processes. As an aldehyde, it can participate in various reactions, including nucleophilic additions and condensation reactions. The compound is of interest in organic synthesis and may serve as an intermediate in the production of pharmaceuticals, agrochemicals, or other fine chemicals. Safety precautions should be taken when handling this substance, as it may pose health risks if inhaled or ingested, and appropriate measures should be implemented to minimize exposure.

Formula: C₉H₉ClO₂

InChI: InChI=1S/C9H9ClO2/c10-5-6-12-9-3-1-8(7-11)2-4-9/h1-4,7H,5-6H2

InChI key: InChIKey=HBHHMVNKQWECIS-UHFFFAOYSA-N

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

Synonyms:

• Benzaldehyde, 4-(2-Chloroethoxy)-
• Benzaldehyde, p-(2-chloroethoxy)-
• N-(2-chloroethoxy)benzaldehyde
• p-(2-Chloroethoxy)benzaldehyde
• 4-(2-Chloroethoxy)benzaldehyde

Benzaldehyde, 4-(2-chloroethoxy)-

CAS: 54373-15-8

Formula: C₉H₉ClO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 184.6196

Ref: IN-DA00I9PQ

4-(2-Chloroethoxy)benzaldehyde

CAS: 54373-15-8

4-(2-Chloroethoxy)benzaldehyde

Purity: 98%

Molecular weight: 184.61956g/mol

Ref: 54-OR10420

4-(2-Chloroethoxy)benzaldehyde

CAS: 54373-15-8

Formula: C₉H₉ClO₂

Purity: 98%

Color and Shape: Liquid, No data available.

Molecular weight: 184.62

Ref: 10-F239984

4-(2-Chloroethoxy)benzaldehyde

CAS: 54373-15-8

4-(2-Chloroethoxy)benzaldehyde is a phenolic compound that has been shown to have antioxidant properties. It can scavenge free radicals and inhibit lipid peroxidation through its electron donating activity. 4-(2-Chloroethoxy)benzaldehyde has also been shown to have anti-inflammatory, anticancer, antifungal, and antimicrobial properties in vitro. The biological activities of this compound are most likely due to its synthesis of heterocycles and functionalities. 4-(2-Chloroethoxy)benzaldehyde has been found in the etoac extract of Moringa oleifera leaves as well as other solvents.

Formula: C₉H₉ClO₂

Purity: Min. 95%

Molecular weight: 184.62 g/mol

Ref: 3D-ECA37315