Product Name:(S)-Ethyl 2-amino-3-(4-fluorophenyl)propanoate hydrochloride

IUPAC Name:ethyl (2S)-2-amino-3-(4-fluorophenyl)propanoate hydrochloride

CAS:1534-90-3
Molecular Formula:C11H15ClFNO2
Purity:95%
Catalog Number:CM100671
Molecular Weight:247.69

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Product Details

CAS NO:1534-90-3
Molecular Formula:C11H15ClFNO2
Melting Point:-
Smiles Code:O=C(OCC)[C@@H](N)CC1=CC=C(F)C=C1.[H]Cl
Density:
Catalog Number:CM100671
Molecular Weight:247.69
Boiling Point:
MDL No:MFCD02259530
Storage:Keep in inert atmosphere, store at room temperature.

Category Infos

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.
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Product Other Information

Product Overview (S)-Ethyl 2-amino-3-(4-fluorophenyl)propanoate hydrochloride, also known as S-EAPF-HCl, is a synthetic compound that has been used in a variety of scientific research applications. It is a chiral amino acid derivative and is used as a building block for a variety of peptide and peptidomimetic drugs. S-EAPF-HCl has been studied in a wide range of fields such as biochemistry, pharmacology, and medicinal chemistry.
Synthesis and Application The synthesis of (S)-Ethyl 2-amino-3-(4-fluorophenyl)propanoate hydrochloride begins with the reaction of ethyl 2-amino-3-fluorobutyrate and 4-fluorophenylboronic acid in the presence of a palladium catalyst. The resulting product is then reacted with hydrochloric acid to form the desired compound. The reaction is conducted in aqueous media at room temperature and is highly efficient, with yields of up to 99%. (S)-Ethyl 2-amino-3-(4-fluorophenyl)propanoate hydrochloride has been used in a variety of scientific research applications. It has been used as a building block for a variety of peptide and peptidomimetic drugs, as well as for the synthesis of small molecules and polymers. It has also been used as a starting material for the synthesis of a variety of drugs, such as antibiotics, antifungals, and antivirals. Additionally, it has been used to study the structure-activity relationships of peptides and peptidomimetics, as well as to study the mechanisms of action of various drugs.
Future Directions The potential future directions for (S)-Ethyl 2-amino-3-(4-fluorophenyl)propanoate hydrochloride include further research into its biochemical and physiological effects, as well as its potential therapeutic applications. Additionally, further research into its structure-activity relationships and mechanisms of action may lead to the development of more effective drugs and therapies. Additionally, further research into its synthesis methods may lead to the development of more efficient and cost-effective methods of production. Finally, further research into its potential toxicity and side effects may lead to the development of safer and more effective drugs.