CAS 51264-69-8

Ethyl 4-formylphenoxyacetate

Description:

Ethyl 4-formylphenoxyacetate, with the CAS number 51264-69-8, is an organic compound characterized by its ester functional group and aromatic structure. It features a phenoxy group, which is a phenyl ring bonded to an oxygen atom, and an aldehyde group (-CHO) attached to the aromatic ring. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. Ethyl 4-formylphenoxyacetate is known for its potential applications in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its reactivity and ability to participate in various chemical reactions, such as nucleophilic substitutions and condensation reactions. It may also exhibit biological activity, making it of interest in medicinal chemistry. As with many organic compounds, handling should be done with care, considering safety data sheets for proper guidelines on toxicity and environmental impact.

Formula: C₁₁H₁₂O₄

InChI: InChI=1S/C11H12O4/c1-2-14-11(13)8-15-10-5-3-9(7-12)4-6-10/h3-7H,2,8H2,1H3

InChI key: InChIKey=CGEOWJVEIAILOR-UHFFFAOYSA-N

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

Synonyms:

• (4-Formyl-phenoxy)-acetic acid ethyl ester
• Acetic Acid, 2-(4-Formylphenoxy)-, Ethyl Ester
• Acetic acid, (4-formylphenoxy)-, ethyl ester
• Acetic acid, (p-formylphenoxy)-, ethyl ester
• Ethyl 2-(4-formylphenoxy)acetate
• Ethyl 4-formylphenoxyacetate
• NSC 156554

4-Formylphenoxyacetic acid ethyl ester

CAS: 51264-69-8

Formula: C₁₁H₁₂O₄

Purity: 95%

Molecular weight: 208.2106

Ref: IN-DA00DCWK

Ethyl (4-formylphenoxy)acetate

CAS: 51264-69-8

Ethyl (4-formylphenoxy)acetate

Purity: 95%

Ref: 54-OR1038673

ethyl (4-formylphenoxy)acetate

CAS: 51264-69-8

Formula: C₁₁H₁₂O₄

Purity: 95+%

Color and Shape: Solid

Molecular weight: 208.213

Ref: 10-F314902

Ethyl (4-formylphenoxy)acetate

CAS: 51264-69-8

Ethyl (4-formylphenoxy)acetate is a molecule that belongs to the group of quinoline derivatives. It is a copper complex that has shown cytotoxic activity against cancer cells in vitro. The cytotoxicity of ethyl (4-formylphenoxy)acetate has been attributed to its ability to form conjugates with monoclonal antibodies, which may be important for treatment and diagnosis of cancer. Studies have demonstrated the interaction between ethyl (4-formylphenoxy)acetate and DNA, as well as the application of radiation and crystallography techniques to optimize labeling.

Formula: C₁₁H₁₂O₄

Purity: Min. 95%

Molecular weight: 208.21 g/mol

Ref: 3D-BCA26469