CAS 14062-29-4

Ethyl (3-chlorophenyl)acetate

Description:

Ethyl (3-chlorophenyl)acetate, with the CAS number 14062-29-4, is an organic compound characterized by its ester functional group. It is formed from the reaction of ethyl alcohol and 3-chlorophenylacetic acid. This compound typically appears as a colorless to pale yellow liquid with a pleasant, fruity odor, making it useful in flavoring and fragrance applications. Ethyl (3-chlorophenyl)acetate is moderately soluble in water and more soluble in organic solvents, reflecting its hydrophobic nature due to the aromatic ring. The presence of the chlorine atom on the phenyl ring can influence its reactivity and biological activity, potentially enhancing its antimicrobial properties. In terms of safety, it is important to handle this compound with care, as it may cause irritation to the skin and eyes. Additionally, proper storage in a cool, well-ventilated area away from heat sources is recommended to maintain its stability and prevent degradation. Overall, this compound is of interest in both industrial applications and research settings.

Formula: C₁₀H₁₁ClO₂

InChI: InChI=1/C10H11ClO2/c1-2-13-10(12)7-8-4-3-5-9(11)6-8/h3-6H,2,7H2,1H3

SMILES: CCOC(=O)Cc1cccc(c1)Cl

Synonyms:

• Benzeneacetic Acid, 3-Chloro-, Ethyl Ester
• Ethyl m-chlorophenylacetate

Benzeneacetic acid, 3-chloro-, ethyl ester

CAS: 14062-29-4

Formula: C₁₀H₁₁ClO₂

Purity: 97%

Color and Shape: Liquid

Molecular weight: 198.6461

Ref: IN-DA001CLB

Ethyl 3-chlorophenylacetate

CAS: 14062-29-4

Ethyl 3-chlorophenylacetate

Purity: 98%

Molecular weight: 198.65g/mol

Ref: 54-OR953372

(3-Chlorophenyl)acetic acid ethyl ester

CAS: 14062-29-4

Formula: C₁₀H₁₁ClO₂

Purity: 95%

Color and Shape: Liquid

Molecular weight: 198.65

Ref: 10-F234440

Ethyl 2-(3-chlorophenyl)acetate

CAS: 14062-29-4

Ethyl 2-(3-chlorophenyl)acetate is an orally active small molecule that has been shown to have a potent immunosuppressive activity in mice. It inhibits the production of antibodies and T cells by binding to the antibody-producing cells in the spleen. Ethyl 2-(3-chlorophenyl)acetate also blocks the production of interleukin-4, which is important for eosinophil activation, and it can be used for asthma treatment. This compound is a competitive antagonist of histamine H1 receptors and has been shown to be a bronchodilator in murine models of asthma.

Formula: C₁₀H₁₁ClO₂

Purity: Min. 95%

Molecular weight: 198.65 g/mol

Ref: 3D-PAA06229