(alphaR,betaS)-rel-beta-Amino-alpha-hydroxybenzenepropanoic acid - Names and Identifiers
Name | (2R,3S)-3-phenylisoserine methyl ester
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Synonyms | Methyl (2R,3S)-3-phenylisoserinate (2R,3S)-Phenylisoserine methylester (2R,3S)-3-phenylisoserine methyl ester Methyl (2R,3S)-3-amino-2-hydroxy-3-phenylpropanoate (2R,3S)-Methyl 3-aMino-2-hydroxy-3-phenylpropanoate 3-amino-2-hydroxy-3-phenylpropanoic acid methyl ester (alphaR,betaS)-rel-beta-Amino-alpha-hydroxybenzenepropanoic acid Benzenepropanoic acid, β-amino-α-hydroxy-, methyl ester, (αR,βS)-rel- (alphaR,betaS)-rel-beta-Amino-alpha-hydroxybenzenepropanoic acid methyl ester benzenepropanoic acid, beta-amino-alpha-hydroxy-, methyl ester, (alphaR,betaS)-
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CAS | 131968-74-6
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EINECS | 1806241-263-5 |
InChI | InChI=1/C10H13NO3/c1-14-10(13)9(12)8(11)7-5-3-2-4-6-7/h2-6,8-9,12H,11H2,1H3/t8-,9+/m0/s1 |
(alphaR,betaS)-rel-beta-Amino-alpha-hydroxybenzenepropanoic acid - Physico-chemical Properties
Molecular Formula | C10H13NO3
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Molar Mass | 195.22 |
Density | 1.212±0.06 g/cm3(Predicted) |
Melting Point | 87-88℃ |
Boling Point | 343.0±42.0 °C(Predicted) |
Flash Point | 161.256°C |
Vapor Presure | 0mmHg at 25°C |
pKa | 10.35±0.45(Predicted) |
Storage Condition | 2-8°C |
Refractive Index | 1.557 |
(alphaR,betaS)-rel-beta-Amino-alpha-hydroxybenzenepropanoic acid - Introduction
(2R,3S)-3-phenylisoserine methyl ester is an organic compound. It is a chiral molecule with two stereocenters, one in the R configuration and the other in the S configuration. Its molecular formula is C11H13NO2.
Regarding its properties,(2R,3S)-3-phenylisoserine methyl ester is a colorless to pale yellow solid. It has a melting point of about 115-117°C. It is stable at room temperature and dissolves in many organic solvents, such as ethanol and ether.
This compound has certain applications in biochemistry. For example, in the synthesis of polypeptides and proteins, methyl (2R,3S)-3-phenylisoserine is used as a chiral starting material. It can also be used as a synthetic raw material for pharmaceutical intermediates.
The method of preparing methyl (2R,3S)-3-phenylisoserine is usually achieved by chemical synthesis. One common method is by stereoselective reaction of alanine methyl ester.
For safety information, limited information is available regarding the toxicity and harmfulness of (2R,3S)-3-phenylisoserine methyl ester. However, as a chemical, it should be used in accordance with appropriate laboratory procedures and safety practices, including the wearing of appropriate personal protective equipment. During use, storage and disposal, the relevant safety operation and regulations shall be strictly observed. Before use, it is recommended to understand the safety data sheet of the compound in detail or consult with the relevant professional.
Last Update:2024-04-09 21:54:55