4313-70-6
(S)-2-Amino-3-(4-ethylphenyl)propanoic acid
CAS: 4313-70-6
Molecular Formula: C11H15NO2
4313-70-6 - Names and Identifiers
| Name | (S)-2-Amino-3-(4-ethylphenyl)propanoic acid |
| Synonyms | H-L-Phe(4-Et)-OH L-p-ethylphenylalanine 4-Ethyl-L-phenylalanine L-Phenylalanine,4-ethyl- L-phenylalanine, 4-ethyl- (S)-2-AMINO-3-(4-ETHYLPHENYL)PROPANOIC ACID (S)-2-Amino-3-(4-ethylphenyl)propanoic acid (S)-2-amino-3-(4-ethylphenyl)propanoic acid(WXG01680) |
| CAS | 4313-70-6 |
| InChI | InChI=1/C11H15NO2/c1-2-8-3-5-9(6-4-8)7-10(12)11(13)14/h3-6,10H,2,7,12H2,1H3,(H,13,14)/t10-/m0/s1 |
4313-70-6 - Physico-chemical Properties
| Molecular Formula | C11H15NO2 |
| Molar Mass | 193.24 |
| Density | 1.135±0.06 g/cm3(Predicted) |
| Melting Point | 244-247 °C (decomp) |
| Boling Point | 335.4±30.0 °C(Predicted) |
| Flash Point | 156.7°C |
| Vapor Presure | 4.72E-05mmHg at 25°C |
| pKa | 2.23±0.10(Predicted) |
| Refractive Index | 1.559 |
4313-70-6 - Introduction
(S)-2-Amino-3-(4-ethylphenyl)propanoic acid is an organic compound with the chemical formula C12H17NO2. It is a chiral compound and has one chiral carbon atom, so two isomers exist, namely (S)-2-Amino-3-(4-ethylphenyl)propanoic acid and (R)-2-amino -3-(4-ethylphenyl) propionic acid.
(S)-2-Amino-3-(4-ethylphenyl)propanoic acid is commonly used as a chiral reagent in organic synthesis reactions and can participate in esterification, amidation, aminolysis and other reactions. It is usually used in the preparation of drugs, ligands, catalysts and other organic intermediates.
The method for preparing (S)-2-Amino-3-(4-ethylphenyl)propanoic acid can be obtained by symmetric synthesis or asymmetric synthesis. Symmetric synthesis refers to the synthesis of target compounds through symmetric chiral raw materials, while asymmetric synthesis uses chiral catalysts or chiral reagents to introduce chirality.
Regarding the safety information of (S)-2-Amino-3-(4-ethylphenyl)propanoic acid, according to the current limited information, it has no clear toxicity and hazard records. However, as an organic compound, it may cause certain toxicity or irritation to the organism, so corresponding safety measures should be taken in use, such as wearing gloves, glasses and protective clothing, and operating in a well-ventilated environment. At the same time, avoid direct contact with skin and eyes, and avoid inhaling its dust or vapor. If contact or inhalation occurs, rinse immediately with water and seek medical help. Relevant chemical safety practices should be followed during handling and storage. It is best to operate in a specialized laboratory or by experienced personnel.
(S)-2-Amino-3-(4-ethylphenyl)propanoic acid is commonly used as a chiral reagent in organic synthesis reactions and can participate in esterification, amidation, aminolysis and other reactions. It is usually used in the preparation of drugs, ligands, catalysts and other organic intermediates.
The method for preparing (S)-2-Amino-3-(4-ethylphenyl)propanoic acid can be obtained by symmetric synthesis or asymmetric synthesis. Symmetric synthesis refers to the synthesis of target compounds through symmetric chiral raw materials, while asymmetric synthesis uses chiral catalysts or chiral reagents to introduce chirality.
Regarding the safety information of (S)-2-Amino-3-(4-ethylphenyl)propanoic acid, according to the current limited information, it has no clear toxicity and hazard records. However, as an organic compound, it may cause certain toxicity or irritation to the organism, so corresponding safety measures should be taken in use, such as wearing gloves, glasses and protective clothing, and operating in a well-ventilated environment. At the same time, avoid direct contact with skin and eyes, and avoid inhaling its dust or vapor. If contact or inhalation occurs, rinse immediately with water and seek medical help. Relevant chemical safety practices should be followed during handling and storage. It is best to operate in a specialized laboratory or by experienced personnel.
Last Update：2024-04-09 21:32:41
