(2S,3S)-2-Amino-3-methoxybutanoic acid - Names and Identifiers
Name | (2S,3S)-2-Amino-3-methoxybutanoic acid
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Synonyms | allothr(me) H-Allo-Thr(Me)-OH O-Methyl-L-allothreonine L-Allothreonine, O-methyl- L-allothreonine, O-methyl- dl-Erythro-O-methylthreonine 2-ammonio-3-methoxybutanoate (2S,3S)-2-Amino-3-methoxybutanoic acid (2S,3S)-2-AMINO-3-METHOXYBUTANOIC ACID, 98
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CAS | 104195-80-4
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InChI | InChI=1/C5H11NO3/c1-3(9-2)4(6)5(7)8/h3-4H,6H2,1-2H3,(H,7,8)/t3-,4-/m0/s1 |
(2S,3S)-2-Amino-3-methoxybutanoic acid - Physico-chemical Properties
Molecular Formula | C5H11NO3
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Molar Mass | 133.15 |
Density | 1.2510 (rough estimate) |
Melting Point | 220-224 °C |
Boling Point | 245.66°C (rough estimate) |
Specific Rotation(α) | 27.5 º (c=0.6, 6N HCl 25 ºC) |
Flash Point | 103.8°C |
Water Solubility | soluble |
Vapor Presure | 0.008mmHg at 25°C |
Appearance | Flakes |
Color | White |
pKa | 2.12±0.10(Predicted) |
Storage Condition | Keep in dark place,Inert atmosphere,Room temperature |
Refractive Index | 1.4206 (estimate) |
(2S,3S)-2-Amino-3-methoxybutanoic acid - Risk and Safety
Safety Description | 24/25 - Avoid contact with skin and eyes.
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HS Code | 29225000 |
(2S,3S)-2-Amino-3-methoxybutanoic acid - Introduction
(2S,3S)-2-amino-3-methoxybutyric acid, also known as amino-3-methoxybutyric acid, is an organic compound. The following is a detailed description of the properties, uses, preparation and safety information of the compound:
Nature:
(2S,3S)-2-amino-3-methoxybutyric acid is a colorless or white solid, stable at room temperature, soluble in water and some organic solvents. It has two asymmetric carbon atoms, so there are four possible stereoisomers. The (2S,3S) isomer in this compound has a specific spatial arrangement.
Use:
(2S,3S)-2-amino-3-methoxybutyric acid is widely used in chemical synthesis. It can be used as an intermediate in the synthesis of other compounds, especially in the field of pharmaceutical synthesis. It can also be used for asymmetric synthesis in organic synthesis reactions or as a chiral inducer.
Preparation Method:
(2S,3S)-2-amino-3-methoxybutanoic acid can be synthesized in a variety of ways. The most commonly used method is to use chiral catalysts to selectively react its functional groups. These catalysts can convert a chemical reactant having a specific stereostructure into a product of a specific stereoisomer.
Safety Information:
The exact safety information about (2S,3S)-2-amino-3-methoxybutyric acid may be limited, so caution should be exercised when using and handling this compound. In general, organic compounds can be potentially dangerous, including potential risks to human health and environmental effects. Therefore, when handling and handling this compound, it is necessary to use personal protective equipment correctly and follow correct laboratory operating procedures. For specific safety information and operational recommendations, it is best to consult the chemical supplier or relevant professional body.
Last Update:2024-04-09 21:54:55