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Merck

423424

Sigma-Aldrich

2-(三甲基硅氧基)-1,3-环己二烯

95%

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About This Item

经验公式(希尔记法):
C9H16OSi
CAS号:
分子量:
168.31
Beilstein:
2079140
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

95%

形狀

liquid

折射率

n20/D 1.462 (lit.)

bp

65 °C/7 mmHg (lit.)

密度

0.899 g/mL at 25 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

C[Si](C)(C)OC1=CCCC=C1

InChI

1S/C9H16OSi/c1-11(2,3)10-9-7-5-4-6-8-9/h5,7-8H,4,6H2,1-3H3

InChI 密鑰

WPIRVUXAMPRMAY-UHFFFAOYSA-N

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一般說明

2-(Trimethylsiloxy)-1,3-cyclohexadiene ((cyclohexa-1,5-dien-1-yloxy)trimethylsilane) is silyl enol ether of cyclohexenone. The Diels–Alder reactions with dienophiles α-acetoxyacrylonitrile, acrylonitrile and α-chloroacrylonitrile has been studied.

應用

2-(Trimethylsiloxy)-1,3-cyclohexadiene may be used as a diene in the synthesis of isoquinuclidinone 2-aza[2.2.2]octa-3,5-dione by reacting with p-toluenesulfonyl cyanide.

象形圖

Flame

訊號詞

Warning

危險聲明

危險分類

Flam. Liq. 3

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

116.6 °F - closed cup

閃點(°C)

47 °C - closed cup

個人防護裝備

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


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分析证书(COA)

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其他客户在看

Safety Assessment of Diels-Alder Reactions with Highly Reactive Acrylic Monomers.
Abele S, et al.
Organic Process Research & Development, 16(12), 2015-2020 (2012)
Design and Scale-Up of Diels-Alder Reactions for the Practical Synthesis of 5-Phenylbicyclo [2.2. 2] oct-5-en-2-one.
Funel JA, et al.
Organic Process Research & Development, 15(6), 1420-1427 (2011)
High-Temperature Diels-Alder Reactions: Transfer from Batch to Continuous Mode.
Abele S, et al.
Organic Process Research & Development, 16(5), 1114-1120 (2011)
Cynthia K McClure et al.
The Journal of organic chemistry, 68(21), 8256-8257 (2003-10-11)
The hetero-Diels-Alder reaction of an electron-deficient nitrile, p-toluenesulfonyl cyanide, with the silyl enol ether of cyclohexenone produced a hydrolytically sensitive [4 + 2] adduct in good yield. Use of Mander's reagent, ethyl cyanoformate, with the same diene, produced an unstable

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