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Merck
CN

E49606

3-乙基甲苯

99%

别名:

1-乙基-3-甲基苯

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线性分子式:
C2H5C6H4CH3
化学文摘社编号:
分子量:
120.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-626-8
Beilstein/REAXYS Number:
1850821
MDL number:
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产品名称

3-乙基甲苯, 99%

InChI key

ZLCSFXXPPANWQY-UHFFFAOYSA-N

InChI

1S/C9H12/c1-3-9-6-4-5-8(2)7-9/h4-7H,3H2,1-2H3

SMILES string

CCc1cccc(C)c1

assay

99%

form

liquid

autoignition temp.

896 °F

refractive index

n20/D 1.496 (lit.)

bp

158-159 °C (lit.)

density

0.865 g/mL at 25 °C (lit.)

Quality Level

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Application

3-乙基甲苯通常被用作一种模型烷基苯衍生物,用于键活化和C(sp3)-H 官能化研究。

pictograms

Flame

signalword

Warning

hcodes

Hazard Classifications

Flam. Liq. 3

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

100.4 °F - closed cup

flash_point_c

38 °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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A Metal?Free Oxidative Dehydrogenative Diels?Alder Reaction for Selective Functionalization of Alkylbenzenes.
Manna S and Antonchick A P
Chemistry?A European Journal , 23(32), 7825-7829 (2017)
Mechanism of C? H Bond Activation of Alkyl-Substituted Benzenes by Cationic Platinum (II) Complexes.
Driver T G, et al.
Organometallics, 24(15), 3644-3654 (2005)
Cu-Facilitated C? O Bond Formation Using N-Hydroxyphthalimide: Efficient and Selective Functionalization of Benzyl and Allylic C? H Bonds.
Lee J M, et al.
Journal of the American Chemical Society, 130(25), 7824-7825 (2008)
Laura Vallecillos et al.
The Science of the total environment, 666, 235-244 (2019-02-25)
This study describes the implementation of a passive sampling-based method followed by thermal desorption gas-chromatography-mass spectrometry (TD-GC-MS) for the monitoring of volatile organic compounds (VOCs) in industrial atmospheres. However, in order to employ passive sampling as a reliable sampling technique
G M Whited et al.
Journal of bacteriology, 166(3), 1028-1039 (1986-06-01)
Pseudomonas putida BG1 was isolated from soil by enrichment with p-toluate and selection for growth with p-xylene. Other hydrocarbons that served as growth substrates were toluene, m-xylene, 3-ethyltoluene, and 1,2,4-trimethylbenzene. The enzymes responsible for growth on these substrates are encoded

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