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110779

Sigma-Aldrich

亚乙基环己烷

99%

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About This Item

线性分子式:
C6H10(=CHCH3)
CAS号:
1003-64-1
分子量:
110.20
EC號碼:
213-711-8
MDL號碼:
MFCD00001662
分類程式碼代碼:
12352100
PubChem物質ID:
24847003
NACRES:
NA.22

化驗

99%

折射率

n20/D 1.462 (lit.)

bp

136 °C (lit.)

密度

0.822 g/mL at 25 °C (lit.)

SMILES 字串

C\C=C1\CCCCC1

InChI

1S/C8H14/c1-2-8-6-4-3-5-7-8/h2H,3-7H2,1H3

InChI 密鑰

BPBOWYWUOUJKLO-UHFFFAOYSA-N

相关类别

一般說明

Ethylidenecyclohexane is oxidized by purified ethylbenzene dehydrogenase.

應用

Ethylidenecyclohexane has been used as a substrate in the Lewis-acid catalyzed reactions of azodicarboxylates with different alkenes.

象形圖

Flame
GHS02

訊號詞

Warning

危險聲明

H226

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）

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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分析证书(COA)

Lot/Batch Number
MKCN1644
MKCL7085
MKCL5594
MKBH6738V
MKBF6748V

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H A Johnson et al.
Journal of bacteriology, 183(15), 4536-4542 (2001-07-10)
The first step in anaerobic ethylbenzene mineralization in denitrifying Azoarcus sp. strain EB1 is the oxidation of ethylbenzene to (S)-(-)-1-phenylethanol. Ethylbenzene dehydrogenase, which catalyzes this reaction, is a unique enzyme in that it mediates the stereoselective hydroxylation of an aromatic
Pompiliu S Aburel et al.
Organic & biomolecular chemistry, 3(12), 2344-2349 (2005-07-13)
Lewis acids such as Cu(OTf)(2), Zn(OTf)(2), Yb(OTf)(3) and Nd(OTf)(3) catalyze the aza-ene reaction of alkenes with azodicarboxylates, giving the allylic amination adducts. The use of bis(2,2,2-trichloroethyl)azodicarboxylate as the amination reagent and Cu(OTf)(2) and Yb(OTf)(3) as the catalysts gave the aza-ene

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