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235040

Sigma-Aldrich

1-苯基-1-三甲基硅氧乙烯

98%

同義詞:

α-(三甲基硅氧基)苯乙烯, 1-苯基-1-三甲硅氧基乙烯

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About This Item

線性公式:
C6H5C(=CH2)OSi(CH3)3
CAS號碼:
分子量::
192.33
Beilstein:
1306914
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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蒸汽密度

>1 (vs air)

品質等級

化驗

98%

形狀

liquid

折射率

n20/D 1.502 (lit.)

bp

88-89 °C/11 mmHg (lit.)

密度

0.938 g/mL at 25 °C (lit.)

官能基

phenyl

儲存溫度

2-8°C

SMILES 字串

C[Si](C)(C)OC(=C)c1ccccc1

InChI

1S/C11H16OSi/c1-10(12-13(2,3)4)11-8-6-5-7-9-11/h5-9H,1H2,2-4H3

InChI 密鑰

AFFPCIMDERUIST-UHFFFAOYSA-N

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一般說明

1-Phenyl-1-trimethylsiloxyethylene is a styrene type silyl enol ether, reacts with formaldehyde and 2,4-pentanedione to yield the corresponding dihydropyran[1]. It also undergoes Mukaiyama aldol reaction with aldehydes in water in the presence of amphiphilic calix[6]arene derivatives as surfactants[2].

應用

1-Phenyl-1-trimethylsiloxyethylene has been used in the synthesis of:
  • β-amino ketones in water via Mannich-type reaction[3]
  • cis-2,6-disubstituted dihydropyrans via three-component, one-pot cascade reaction[4]

象形圖

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訊號詞

Warning

危險聲明

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

168.8 °F - closed cup

閃點(°C)

76 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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分析證明 (COA)

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客戶也查看了

Calix [6] arene derivatives bearing sulfonate and alkyl groups as surfactants in Sc (OTf)3-catalyzed Mukaiyama aldol reactions in water.
Tian H-Y, et al.
Tetrahedron Letters, 41(15), 2529-2532 (2000)
Novel one-pot Mannich-type reaction in water: indium trichloride-catalyzed condensation of aldehydes, amines and silyl enol ethers for the synthesis of ?-amino ketones and esters.
Loh T-P and Wei L-L.
Tetrahedron Letters, 39(3), 323-326 (1998)
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
Catalyst-free aqueous multicomponent domino reactions from formaldehyde and 1, 3-dicarbonyl derivatives.
Gu Y, et al.
Green Chemistry, 11(12), 1968-1972 (2009)

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