21158-73-6

Basic information

• Product Name: (S)-2-AMINO-3-(4-CHLORO-PHENYL)-2-METHYL-PROPIONIC ACID ETHYL ESTER
• Synonyms: (S)-2-AMINO-3-(4-CHLORO-PHENYL)-2-METHYL-PROPIONIC ACID ETHYL ESTER;ALANINE, 3-(P-CHLOROPHENYL)-2-METHYL, ETHYL ESTER;ethyl 2-amino-3-(4-chlorophenyl)-2-methylpropanoate
• CAS NO: 21158-73-6
• Molecular Formula: C12H16ClNO2
• Molecular Weight: 241.71
• Mol File: 21158-73-6.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 163-164 °C(Press: 4-5 Torr)
• Appearance: /
• Density: 1.165±0.06 g/cm3(Predicted)
• PKA: 7.23±0.25(Predicted)
• CAS DataBase Reference: (S)-2-AMINO-3-(4-CHLORO-PHENYL)-2-METHYL-PROPIONIC ACID ETHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-AMINO-3-(4-CHLORO-PHENYL)-2-METHYL-PROPIONIC ACID ETHYL ESTER(21158-73-6)
• EPA Substance Registry System: (S)-2-AMINO-3-(4-CHLORO-PHENYL)-2-METHYL-PROPIONIC ACID ETHYL ESTER(21158-73-6)

Safety Data

• Hazardous Substances Data: 21158-73-6(Hazardous Substances Data)

Usage

Description

(S)-2-AMINO-3-(4-CHLORO-PHENYL)-2-METHYL-PROPIONIC ACID ETHYL ESTER is a chiral ethyl ester derivative of (S)-2-amino-3-(4-chlorophenyl)-2-methylpropanoic acid. (S)-2-AMINO-3-(4-CHLORO-PHENYL)-2-METHYL-PROPIONIC ACID ETHYL ESTER is characterized by its non-superimposable mirror image, with the (S) enantiomer being the active form. Its chiral structure and potential biological activity make it a compound of interest for pharmaceuticals and research. It can serve as a starting material or intermediate in organic synthesis, and its properties and reactivity are valuable to chemists and researchers. The specific uses and properties of (S)-2-AMINO-3-(4-CHLORO-PHENYL)-2-METHYL-PROPIONIC ACID ETHYL ESTER may vary depending on the enantiomer and its intended application.

Uses

Used in Pharmaceutical Industry:
(S)-2-AMINO-3-(4-CHLORO-PHENYL)-2-METHYL-PROPIONIC ACID ETHYL ESTER is used as a chiral compound for its potential applications in the development of pharmaceutical products. Its unique structure may contribute to the creation of new drugs or the enhancement of existing ones, particularly in the areas where chirality plays a crucial role in the compound's activity and efficacy.
Used in Research and Development:
In the field of research and development, (S)-2-AMINO-3-(4-CHLORO-PHENYL)-2-METHYL-PROPIONIC ACID ETHYL ESTER is used as a starting material or intermediate for organic synthesis. Its reactivity and properties make it a valuable tool for chemists and researchers working on the synthesis of new compounds or the improvement of existing synthetic routes.
Used in Chiral Chemistry:
(S)-2-AMINO-3-(4-CHLORO-PHENYL)-2-METHYL-PROPIONIC ACID ETHYL ESTER is used as a chiral building block for the synthesis of enantiomerically pure compounds. Its (S) enantiomer's activity makes it a potentially important component in the development of enantiomerically selective reactions and the creation of chiral molecules with specific biological activities.
Used in Organic Synthesis:
As an ethyl ester derivative, (S)-2-AMINO-3-(4-CHLORO-PHENYL)-2-METHYL-PROPIONIC ACID ETHYL ESTER is used as a versatile intermediate in organic synthesis. Its functional groups can be further modified or reacted to produce a variety of target molecules, making it a valuable asset in the synthesis of complex organic compounds.