2,2-Dimethoxy-1-(prop-2-en-1-yl)-1,2-azasilolidine - Names and Identifiers
Name | 1-allyl-2,2-dimethoxy-azasilolidine
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Synonyms | LogP 1-allyl-2,2-dimethoxy-azasilolidine 2,2-Dimethoxy-1-(prop-2-en-1-yl)-1,2-azasilolidine 1-Aza-2-silacyclopentane, 2,2-dimethoxy-1-(2-propen-1-yl)-
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CAS | 618914-49-1
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InChI | InChI=1/C8H17NO2Si/c1-4-6-9-7-5-8-12(9,10-2)11-3/h4H,1,5-8H2,2-3H3 |
2,2-Dimethoxy-1-(prop-2-en-1-yl)-1,2-azasilolidine - Physico-chemical Properties
Molecular Formula | C8H17NO2Si
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Molar Mass | 187.31 |
Boling Point | 52-54°C / 3 |
Sensitive | 8: reacts rapidly with moisture, water, protic solvents |
2,2-Dimethoxy-1-(prop-2-en-1-yl)-1,2-azasilolidine - Introduction
1-allyl-2,2-dimethoxy-azasilolidine is an organic compound with the chemical formula C8H17NO2Si. Here is some information about the compound:
Nature:
-Appearance: colorless or light yellow liquid
-Molecular weight: 187.31g/mol
-Boiling point: about 96-98°C
-Density: about 0.92-0.93 g/mL
Use:
1-allyl-2,2-dimethoxy-azasilolidine is mainly used as a catalyst or reagent in organic synthesis reactions. It can be used in many fields such as polymerization inhibition of diene polymers, transition metal-catalyzed reactions, and synthesis of bioactive molecules.
Preparation Method:
The preparation of 1-allyl-2,2-dimethoxy-azasilolidine can be carried out by the following steps:
1. Chlorodimethylsilane (ClMe2SiH) is reacted with propenyl alcohol to obtain an allylsilane compound.
2. The allylsilane compound is reacted with boron pentafluoride azepine to obtain 1-allyl-2,2-dimethoxy-azasilolidine.
Safety Information:
There is limited safety information regarding 1-allyl-2,2-dimethoxy-azasilolidine. However, as an organic compound, use should take appropriate safety measures and follow laboratory procedures. Avoid contact with skin, eyes and inhalation of vapors during use. Before use, it is recommended to read and follow the safety specification (SDS) of the product. If you have any safety and health concerns, you should consult a professional.
Last Update:2024-04-10 22:29:15