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104195-80-4

(2S,3S)-2-Amino-3-methoxybutanoic acid

CAS: 104195-80-4

Molecular Formula: C5H11NO3

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104195-80-4 - Names and Identifiers

Name (2S,3S)-2-Amino-3-methoxybutanoic acid
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
CAS 104195-80-4
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

104195-80-4 - Physico-chemical Properties

Molecular FormulaC5H11NO3
Molar Mass133.15
Density1.2510 (rough estimate)
Melting Point220-224 °C
Boling Point245.66°C (rough estimate)
Specific Rotation(α)27.5 º (c=0.6, 6N HCl 25 ºC)
Flash Point103.8°C
Water Solubilitysoluble
Vapor Presure0.008mmHg at 25°C
AppearanceFlakes
ColorWhite
pKa2.12±0.10(Predicted)
Storage ConditionKeep in dark place,Inert atmosphere,Room temperature
Refractive Index1.4206 (estimate)

104195-80-4 - Risk and Safety

Safety Description24/25 - Avoid contact with skin and eyes.
HS Code29225000

104195-80-4 - 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
104195-80-4
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Tel: +86-18821248368
Email: Int06@meryer.com
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CAS: 104195-80-4
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View History
104195-80-4
异构体混合物
1,4-二异丙基
丙炔氟草胺
98027-21-5
二甲基二硫
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