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Merck

545236

Sigma-Aldrich

二叔丁基硅烷

97%

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About This Item

线性分子式:
[(CH3)3C]2SiH2
CAS号:
分子量:
144.33
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.22

化驗

97%

折射率

n20/D 1.42 (lit.)

bp

129-130 °C (lit.)

mp

−38 °C (lit.)

密度

0.729 g/mL at 25 °C (lit.)

SMILES 字串

[H][Si]([H])(C(C)(C)C)C(C)(C)C

InChI

1S/C8H20Si/c1-7(2,3)9-8(4,5)6/h9H2,1-6H3

InChI 密鑰

ZLKSBZCITVUTSN-UHFFFAOYSA-N

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應用

Di-tert-butylsilane can be used as a reagent to synthesize:
  • 1,1-di-tert-butyl-N-phenylsilanamine by dehydrogenative coupling with aniline in the presence of supported gold catalyst.
  • Benzyloxy di-tert-butylsilane by dehydrocoupling of benzyl alcohol using NaOH as a catalyst.
  • Di-tert-butyl(3-cyclohexylprop-1-yn-1-yl)silane by silylation reaction with 2-propyn-1-ylcyclohexane using alkali metal hydroxide as a catalyst.

象形圖

Flame

訊號詞

Danger

危險聲明

危險分類

Flam. Liq. 2

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

28.0 °F - closed cup

閃點(°C)

-2.22 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


分析证书(COA)

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Sodium Hydroxide Catalyzed Dehydrocoupling of Alcohols with Hydrosilanes
Toutov AA, et al.
Organic Letters, 18(22), 5776-5779 (2016)
Alkali metal-hydroxide-catalyzed C (sp)-H bond silylation
Toutov AA, et al.
Journal of the American Chemical Society, 139(4), 1668-1674 (2017)
Dehydrogenative Coupling of Hydrosilanes with Amines Using Au/HAP
Uozumi Y and Hamasaka G
Synfacts, 11(05), 0558-0558 (2015)

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