Oxirane, 2-[(1,1-dimethylethoxy)methyl]-, (2S) - Names and Identifiers
Name | S-(+)-TERT-BUTYL GLYCIDYL ETHER
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Synonyms | (S)-t-Butyl glycidyl ether S-(+)-TERT-BUTYL GLYCIDYL ETHER (S)-2-(tert-butoxymethyl)oxirane (2S)-2-(tert-Butoxymethyl)oxirane (2S)-2-[(1,1-dimethylethoxy)methyl]Oxirane Oxirane, 2-[(1,1-dimethylethoxy)methyl]-, (2S) oxirane, 2-[(1,1-dimethylethoxy)methyl]-, (2S)-
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CAS | 130232-97-2
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InChI | InChI=1/C7H14O2/c1-7(2,3)9-5-6-4-8-6/h6H,4-5H2,1-3H3/t6-/m0/s1 |
Oxirane, 2-[(1,1-dimethylethoxy)methyl]-, (2S) - Physico-chemical Properties
Molecular Formula | C7H14O2
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Molar Mass | 130.18 |
Density | 0.944±0.06 g/cm3(Predicted) |
Boling Point | 84-86 °C(Press: 75.0 Torr) |
Flash Point | 43.333°C |
Vapor Presure | 4.561mmHg at 25°C |
Storage Condition | Room Temprature |
Refractive Index | 1.432 |
Oxirane, 2-[(1,1-dimethylethoxy)methyl]-, (2S) - Introduction
(S)-( )-tert-butyl glycidyl ether, chemical name (S)-2-methyl-2-propanyl-1,3-dioxolane, is an organic compound. It is an optically active compound with optical properties, and the optical activity is mainly determined by its stereoisomers.
Tert-butyl glycidyl ether is commonly used as a chiral reagent and as an active substance for enzymes. It is mainly used for the synthesis and separation of chiral alcohols, ketones, aldehydes and other compounds. It can be used as a solvent for chiral catalysts and an adsorbent for chiral solid phase extraction materials.
The preparation method of tert-butyl glycidyl ether generally adopts synthetic chemical methods, usually from tert-butyl alcohol and dimethyl carbonate through redox reaction.
Pay attention to safety when using tert-butyl glycidyl ether. It has low toxicity, but still need to be careful to stay away from fire and avoid inhalation. Work with appropriate protective equipment, such as gloves and goggles, to avoid direct contact. At the same time, should strictly abide by the relevant safety procedures. If taken by mistake or inhaled by mistake, seek medical attention immediately.
Last Update:2024-04-09 21:11:58