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Merck
CN

32008

1,2-二乙苯

≥99.0% (GC)

别名:

邻二乙苯

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线性分子式:
C6H4(C2H5)2
化学文摘社编号:
分子量:
134.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-170-1
Beilstein/REAXYS Number:
1904392
MDL number:
Assay:
≥99.0% (GC)
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产品名称

1,2-二乙苯, ≥99.0% (GC)

InChI key

KVNYFPKFSJIPBJ-UHFFFAOYSA-N

InChI

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

SMILES string

CCc1ccccc1CC

assay

≥99.0% (GC)

autoignition temp.

743 °F

refractive index

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

bp

183 °C (lit.)

mp

−31 °C (lit.)

density

0.88 g/mL at 25 °C (lit.)

Quality Level

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Application

  • 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)。

General description

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

pictograms

Flame

signalword

Warning

hcodes

Hazard Classifications

Flam. Liq. 3

存储类别

3 - Flammable liquids

wgk

WGK 2

flash_point_f

131.0 °F - closed cup

flash_point_c

55 °C - closed cup

ppe

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

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Synthesis of arylbenziodoxoles using pseudocyclic benziodoxole triflate and arenes
Yoshimura A, et al.
ARKIVOC (Gainesville, FL, United States), 2020 (2021)
Formation of 4, 5, 6, 7-tetrahydroisoindoles by palladium-catalyzed hydride reduction
Hou D, et al.
The Journal of Organic Chemistry, 72 (2007)
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)
I Linhart et al.
Xenobiotica; the fate of foreign compounds in biological systems, 26(12), 1263-1272 (1996-12-01)
1. Biotransformation of 1,2-diethenylbenzene (1) in rat was studied. Five urinary metabolites were isolated by extraction of acid hydrolysed urine and identified by nmr and mass spectroscopy, namely, 1-(2-ethenylphenyl)ethane-1,2-diol (2) 2-ethenylmandelic acid (3), 2-ethenylphenylglyoxylic acid (4), 2-ethenylphenylacetylglycine (5) N-acetyl-S-[1-(2-ethenylphenyl)-2-hydroxyethyl]cysteine (6)
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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