(1S,2S)-1,2-Bis(2-methoxyphenyl)ethylenediamine - Names and Identifiers
Name | (1S,2S)-1,2-Bis(2-methoxyphenyl)ethylenediamine
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Synonyms | (1S,2S)-1,2-Bis(2-methoxyphenyl)ethylenediamine (S,S)-1,2-BIS(2-METHOXYPHENYL)-1,2-ETHANEDIAMINE (1S,2S)-1,2-bis(2-Methoxyphenyl)-1,2-ethanediaMine (1S,2S)-1,2-Bis(2-methoxyphenyl)ethane-1,2-diamine 1,2-Ethanediamine, 1,2-bis(2-methoxyphenyl)-, (1S,2S)-
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CAS | 148240-65-7
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(1S,2S)-1,2-Bis(2-methoxyphenyl)ethylenediamine - Physico-chemical Properties
Molecular Formula | C16H20N2O2
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Molar Mass | 272.34 |
Storage Condition | Room Temprature |
(1S,2S)-1,2-Bis(2-methoxyphenyl)ethylenediamine - Introduction
(1S,2S)-1,2-Bis(2-methoxyphenyl)ethylenediamine is an organic compound with the chemical formula C16H20N2O2. The following is an introduction to its nature, use, preparation and safety information:
Nature:
-Appearance: White crystalline solid.
-Melting point: about 115-118°C.
-Solubility: Can be dissolved in organic solvents such as ethanol, dichloromethane and ether.
Use:
- (1S,2S)-1,2-Bis(2-methoxyphenyl)ethylenediamine are commonly used as chiral catalysts and ligands, and are widely used in asymmetric synthesis reactions.
-It can participate in the preparation of chiral acids or chiral transition metal complexes for chiral catalysis and asymmetric catalysis.
Preparation Method:
- (1S,2S)-1,2-Bis(2-methoxyphenyl)ethylenediamine are prepared by many methods, and a common method is to be synthesized by reduction and carbonylation. The specific preparation steps are complex and require synthetic techniques in the chemical laboratory.
Safety Information:
- (1S,2S)-1,2-Bis(2-methoxyphenyl)ethylenediamine there are no clear toxicity data, so it is necessary to take appropriate laboratory safety measures during processing.
-Because it is an organic compound, avoid prolonged or heavy contact with skin and eyes to avoid irritation or other adverse reactions.
-During use or storage, keep it away from fire and oxidizing agents, and place it in a sealed, dry, cool place.
Last Update:2024-04-10 22:29:15