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重要文件

32008

Sigma-Aldrich

1,2-二乙苯

≥99.0% (GC)

同義詞:

邻二乙苯

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About This Item

線性公式:
C6H4(C2H5)2
CAS號碼:
分子量::
134.22
Beilstein:
1904392
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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化驗

≥99.0% (GC)

自燃溫度

743 °F

折射率

n20/D 1.502 (lit.)
n20/D 1.503

bp

183 °C (lit.)

mp

−31 °C (lit.)

密度

0.88 g/mL at 25 °C (lit.)

SMILES 字串

CCc1ccccc1CC

InChI

1S/C10H14/c1-3-9-7-5-6-8-10(9)4-2/h5-8H,3-4H2,1-2H3

InChI 密鑰

KVNYFPKFSJIPBJ-UHFFFAOYSA-N

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一般說明

1,2-二乙基苯可用作反应物,通过分子间傅-克烷基化制备假环式二芳基碘三氟甲磺酸酯,5,6-二取代茚满酮中间体,通过自由基溴化反应制备二溴化物中间体,以及吲哚啉的脱氢化 C-H/C-H芳基化[1][2][3][4]

應用

  • Attraction of adult Harmonia axyridis to volatiles of the insectary plant Cnidium monnieri:研究1,2-二乙基苯对异色瓢虫的吸引,表明在生物防治策略中的应用潜力(Zhiping et al., 2020)。

象形圖

Flame

訊號詞

Warning

危險聲明

防範說明

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 2

閃點(°F)

131.0 °F - closed cup

閃點(°C)

55 °C - closed cup

個人防護裝備

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


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Formation of 4, 5, 6, 7-tetrahydroisoindoles by palladium-catalyzed hydride reduction
Hou D, et al.
The Journal of Organic Chemistry, 72 (2007)
Synthesis of arylbenziodoxoles using pseudocyclic benziodoxole triflate and arenes
Yoshimura A, et al.
ARKIVOC (Gainesville, FL, United States), 2020 (2021)
Exceptionally Mild Palladium (II)-Catalyzed Dehydrogenative C--H/C--H Arylation of Indolines at the C-7 Position under Air
Jiao L, et al.
Organic Letters, 16 (2014)
Jean-Paul Payan et al.
Archives of toxicology, 82(9), 591-600 (2008-02-07)
The bio-distribution of the neurotoxic 1,2-diethylbenzene (1,2-DEB) was studied in male Sprague-Dawley rats after intravenous administration of [(14)C] 1,2-DEB (1 mg kg(-1)). The highest concentrations of [(14)C] non-volatile metabolites, determined by whole-body auto-radiography, were in the nasal cavity, ethmoid turbinates
J P Payan et al.
Drug metabolism and disposition: the biological fate of chemicals, 29(6), 868-876 (2001-05-17)
In a previous study, it was shown that the neurotoxic compound 1,2-diethylbenzene (1,2-DEB) is mainly hydroxylated in the alkyl chain to give 1-(2'-ethylphenyl)ethanol (1,2-EPE) and excreted in urine of rats as two glucuronide compounds (GA1 and GA2). Some findings have

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