CAS:7688-51-9|二(三甲基硅基)烯丙基胺
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产品别名:
N-Allyl-N,N-bis(trimethylsilyl)amine
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CAS 号:
7688-51-9
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分 子 量:
201.46
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分 子 式:
C9H23NSi2
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产品纯度:
≥95%
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产品规格:
500mg,1g(可根据需求定制)
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运输条件:
顺丰速运包邮
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产品说明:
此产品仅用于科研,不能用于人体治疗、药物开发、和其他商业用途。
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更新时间:
2023-02-24 11:23:47
产品名称:二(三甲基硅基)烯丙基胺
英文名称:N-Allyl-N,N-bis(trimethylsilyl)amine
别名:N-烯丙基-N,N-双(三甲基甲硅烷基)胺;3,3',4',5,5',7-六羟基黄酮3-O-鼠李糖苷
规格或纯度:95%
运输条件:常规运输
Application:N-Allyl-N,N-bis(trimethylsilyl)amine or N,N-bis(trimethylsilyl)prop-2-en-1-amine (AHMDS) can be used as a nucleophilic reagent to prepare:• Complex bicyclic scaffolds by reacting with aryl aldehydes via imine formation followed by efficient multicomponent reactions.• Dithiasuccinoyl (Dts) heterocycle by reacting with bisthiocarbamoyl chloride.• Allyl selenide by reacting with aryl selenium salt in the presence of a ruthenium catalyst; Allyl selenide is utilized as a key intermediate in organic synthesis.AHMDS can also be used as a reagent in hydrosilylation and hydroboration reaction. It may be also used as an electrolyte additive.
Application:N-Allyl-N,N-bis(trimethylsilyl)amine or N,N-bis(trimethylsilyl)prop-2-en-1-amine (AHMDS) can be used as a nucleophilic reagent to prepare:• Complex bicyclic scaffolds by reacting with aryl aldehydes via imine formation followed by efficient multicomponent reactions.• Dithiasuccinoyl (Dts) heterocycle by reacting with bisthiocarbamoyl chloride.• Allyl selenide by reacting with aryl selenium salt in the presence of a ruthenium catalyst; Allyl selenide is utilized as a key intermediate in organic synthesis.AHMDS can also be used as a reagent in hydrosilylation and hydroboration reaction. It may be also used as an electrolyte additive.
CAS编号:7688-51-9
敏感性:对湿度敏感
折光率:n20/D 1.440 (lit.)
沸点:72°C/15 mmHg (lit.)
储存温度充氩
MDL号:MFCD00545193
密度:0.816 g/mL at 25 °C (lit.)
分子量:201.46
分子式:C9H23NSi2
货号:Delta-82125
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