Allyltrimethylsilane
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762-72-1C=CC[Si](C)(C)CHYWCXWRMUZYRPH-UHFFFAOYSA-Nused to make allyl C-glycosylic compounds
762-72-1DTXSID5061089化学的特性clear colourless liquid
安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。
Danger
H225 (100%): Highly Flammable liquid and vapor [Danger Flammable liquids]
P210, P233, P240, P241, P242, P243, P261, P264, P264+P265, P271, P280, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 50 reports by companies from 7 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Status: Active Update: 18-11-2019 https://echa.europa.eu/registration-dossier/-/registered-dossier/26053
Allyltrimethylsilane: Does not have an individual approval but may be used under an appropriate group standard
使用Allyltrimethylsilane is a general reagent to introduce allyl groups across acid chlorides, aldehydes, ketones, iminium ions, enones, and for cross-coupling with other carbon electrophiles. It is used as a reagent in HosomiSakurai reaction.
製造方法Allyltrimethylsilane is synthesized by the reaction of trimethylchlorosilane and allylmagnesium bromide.
純化方法Fractionate it through an efficient column at atmospheric pressure. If impure, dissolve it in THF, shake it with H2O (2x), dry (Na2SO4), filter and fractionate it. [Cudlin & Chvalovsky′ Collect Czech Chem Commun 27 1658 1962, Beilstein 4 IV 3927.]
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