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Merck
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重要文件

371440

Sigma-Aldrich

(1--丁基乙烯氧基)三甲基硅烷

98%

同義詞:

(2,2-二甲基-1-亚甲基丙氧基)三甲基硅烷, 3,3-二甲基-2-三甲基硅氧基-1-丁烯, 频哪酮烯醇三甲基硅基醚

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About This Item

線性公式:
(CH3)3CC(=CH2)OSi(CH3)3
CAS號碼:
分子量::
172.34
Beilstein:
2204704
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

98%

形狀

liquid

折射率

n20/D 1.409 (lit.)

bp

140-142 °C (lit.)

密度

0.798 g/mL at 25 °C (lit.)

SMILES 字串

CC(C)(C)C(=C)O[Si](C)(C)C

InChI

1S/C9H20OSi/c1-8(9(2,3)4)10-11(5,6)7/h1H2,2-7H3

InChI 密鑰

PEHJULPJEVIIFJ-UHFFFAOYSA-N

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一般說明

(1-tert-Butylvinyloxy)trimethylsilane is a silyl enol. It belongs to organosilicone class of compounds. Enthalpy of vaporization of (1-tert-Butylvinyloxy)trimethylsilane at boiling point has been reported.

應用

(1-tert-Butylvinyloxy)trimethylsilane ((2,2-Dimethyl-1-methylenepropoxy)trimethylsilane) may be used in the synthesis of cis-3,3-dimethyl-1-(6-phenethyl-3,6-dihydro-2H-pyran-2-yl)butan-2-one.
(1-tert-Butylvinyloxy)trimethylsilane may be used in the preparation of 1-(4-bromophenyl)-4,4-dimethylpentan-3-one.

象形圖

FlameExclamation mark

訊號詞

Warning

危險分類

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

75.2 °F - closed cup

閃點(°C)

24 °C - closed cup

個人防護裝備

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


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分析證明 (COA)

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Yaws CL.
Thermophysical Properties of Chemicals and Hydrocarbons, 574-574 (2014)
Salvatore Ferla et al.
Journal of medicinal chemistry, 57(18), 7702-7715 (2014-08-26)
The synthesis of imidazole styrylbenzamide, tert-butyl styrylimidazole, and tert-butyl styrylsulfonate derivatives is described. Evaluation of binding affinity and inhibitory activity against CYP24A1 identified the imidazole styrylbenzamides as potent inhibitors of CYP24A1, having selectivity with respect to CYP27B1 comparable with or
Robert J Hinkle et al.
Tetrahedron, 65(34), 6834-6839 (2010-02-18)
The rapid synthesis of cis-2,6-disubstituted dihydropyrans is achieved in a three-component, one-pot cascade reaction. BiBr(3)-ediated addition of ketene silyl acetals or silyl enol ethers to beta,gamma-unsaturated cis-4-trimethylsilyl-3-butenal provides a Mukaiyama aldol adduct containing a vinylsilane moiety tethered to a silyl

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