cas 88352-43-6|| where to buy Ethyl 3-(4-chlorobenzamido)-4-(furan-2-yl)-4-oxobutanoate

Nom du produit:Ethyl 3-(4-chlorobenzamido)-4-(furan-2-yl)-4-oxobutanoate

IUPAC Name:ethyl 3-[(4-chlorophenyl)formamido]-4-(furan-2-yl)-4-oxobutanoate

: CAS：88352-43-6; Formule moléculaire：C17H16ClNO5; Pureté：97%

: Numéro de catalogue：CM244262; Poids moléculaire：349.77

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: N° CAS:88352-43-6; Formule moléculaire:C17H16ClNO5; Point de fusion:-; Code SMILES:O=C(OCC)CC(NC(C1=CC=C(Cl)C=C1)=O)C(C2=CC=CO2)=O; Densité:

: Numéro de catalogue:CM244262; Poids moléculaire:349.77; Point d'ébullition:; N° Mdl:; Stockage:

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: Amino Acids and Peptides; Amino acids are organic compounds containing a basic amino group and an acidic carboxyl group. Because amino acids contain both amino and carboxyl groups, they can be polymerized in an end-to-end manner, removing a molecule of water to form a covalent amide bond or peptide bond. Many amino acids are linked together end to end to form a polypeptide. Amino acids and peptides are important components in the fields of medicine and life sciences.; amino acids wholesale; if you are finding amino acids wholesaler in china, we will be your best choose! We have our own factory, so we can give you a cheap price!

: Furans; Furan is a cyclic flammable liquid compound C4H4O that is obtained from wood oils of pines or made synthetically and is used especially in organic synthesis. Furan is aromatic because a pair of lone pair electrons of the oxygen atom in its molecule forms a large π bond in the plane of the conjugated orbital, making a total of 6 electrons in the plane of the conjugated plane, conforming to the 4n+2 structure. Aromaticity makes furan have the property of easy substitution and difficult addition. The other lone pair of electrons in oxygen stretches out. The oxygen atom itself conforms to sp2 hybridization. Due to the presence of the aromatic ring, the chemical behavior of furan is not very similar to that of other unsaturated heterocycles. The oxygen in the aromatic ring has an electron-donating effect, so the electrophilic substitution reactivity of furan is stronger than that of benzene.; Furan | C4H4O | Where to Buy Furans-Chemenu; Furane | Furanes | Furfuran | Furan | C4H4O | Furan Synthesis | Where to Buy Furans; Looking to buy furan? Chemenu offers a diverse selection of high-quality furan compounds. Find the perfect furans for your research or industrial applications. Explore our inventory today!

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Product Overview	Ethyl 3-(4-chlorobenzoylamino)-4-(2-furyl)-4-oxobutyrate is a chemical compound that has gained significant attention in scientific research due to its potential applications in medicine and pharmacology. This compound is also known as ethyl 3-(4-chlorobenzoyl) amino-4-(2-furyl)-4-oxobutanoate, and its chemical formula is C17H16ClNO5.
Synthesis Method	The synthesis of ethyl 3-(4-chlorobenzoylamino)-4-(2-furyl)-4-oxobutyrate involves several steps, including the reaction of 4-chlorobenzoic acid with thionyl chloride to form 4-chlorobenzoyl chloride. This is then reacted with ethyl 3-aminocrotonate to produce ethyl 3-(4-chlorobenzoylamino)-4-chlorocrotonate. The final step involves the reaction of ethyl 3-(4-chlorobenzoylamino)-4-chlorocrotonate with furan-2-carbaldehyde to produce ethyl 3-(4-chlorobenzoylamino)-4-(2-furyl)-4-oxobutyrate.
Scientific Research Application	Ethyl 3-(4-chlorobenzoylamino)-4-(2-furyl)-4-oxobutyrate has been the subject of extensive scientific research due to its potential applications in medicine and pharmacology. It has been found to have anticancer properties and has been studied for its potential use in the treatment of various types of cancer, including breast cancer, lung cancer, and prostate cancer.
Future Directions	There are several future directions for research on ethyl 3-(4-chlorobenzoylamino)-4-(2-furyl)-4-oxobutyrate. One area of research is the development of more efficient synthesis methods to produce this compound. Another area is the investigation of its potential use in combination with other anticancer agents to enhance its effectiveness. Additionally, further research is needed to determine its safety and efficacy in humans, and to develop new methods for delivering this compound to cancer cells.

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