CAS 18325-74-1

ETHYL-2-(3-ALLYL)-4-PENTENOATE

Description:

Ethyl-2-(3-allyl)-4-pentenoate, with the CAS number 18325-74-1, is an organic compound characterized by its ester functional group, which is derived from the reaction of an alcohol (ethanol) and a carboxylic acid. This compound features a pentenoate backbone, indicating the presence of a five-carbon chain with a double bond, and an allyl group, which contributes to its reactivity and potential applications in organic synthesis. Ethyl-2-(3-allyl)-4-pentenoate is typically a colorless to pale yellow liquid with a fruity odor, making it potentially useful in flavor and fragrance applications. Its structure allows for various chemical reactions, including polymerization and cross-linking, which can be exploited in the production of polymers and other materials. Additionally, the presence of the double bond and allyl group may enhance its reactivity in various chemical processes, making it a valuable intermediate in organic synthesis. Safety data should be consulted for handling and storage, as with all chemical substances.

Formula: C₁₀H₁₆O₂

InChI: InChI=1/C10H16O2/c1-4-7-9(8-5-2)10(11)12-6-3/h4-5,9H,1-2,6-8H2,3H3

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

Synonyms:

• Ethyl-2-(2-Allyl)-4-Pentenotate
• Ethyl 2-Prop-2-En-1-Ylpent-4-Enoate

Ethyl 2-allylpent-4-Enoate

CAS: 18325-74-1

Formula: C₁₀H₁₆O₂

Molecular weight: 168.24

Ref: 4Z-P-219049

Diallylacetic Acid Ethyl Ester

Controlled Product

CAS: 18325-74-1

Applications Diallylacetic Acid Ethyl Ester is a reactant used in the synthesis of isopentenyl-N-methylquinolinedione.
References Zikou, L.C., igglessi-Markopoulou, O.: Synthesis, 12, 1861 (2008)

Formula: C₁₀H₁₆O₂

Color and Shape: Neat

Molecular weight: 168.23

Ref: TR-D415995

Diallylacetic Acid Ethyl-d5 Ester

Controlled Product

CAS: 18325-74-1

Formula: C₁₀H₁₁D₅O₂

Color and Shape: Neat

Molecular weight: 288.381

Ref: TR-D415997

Diallylacetic acid ethyl-d5 ester

CAS: 18325-74-1

The diallylacetic acid ethyl-d5 ester is a monomer that belongs to the group of carbocycles. It is synthesized by reacting allyl alcohol with acetic anhydride and ethyl iodide in the presence of triethylstannane. The monomer has been shown to inhibit phagocytosis, which may be due to its interaction with phosphatidylethanolamine or the inhibition of the enzyme cyclooxygenase. Diallylacetic acid ethyl-d5 ester also has antibacterial properties and can inhibit heterocycles and other organic compounds, such as tributylstannane. Diallylacetic acid ethyl-d5 ester has not been shown to have any immunopotentiating effects.

Formula: C₁₀H₁₆O₂

Purity: Min. 95%

Molecular weight: 168.23 g/mol

Ref: 3D-TAA32574