Factory sells 1-TERT-BUTYL-4-ETHYLBENZENE 7364-19-4 with sufficient production capacity
- Molecular Formula: C12H18
- Molecular Weight: 162.275
- Vapor Pressure: 0.264mmHg at 25°C
- Melting Point: -38.35°C
- Refractive Index: 1.4933
- Boiling Point: 211.5°Cat760mmHg
- Flash Point: 75.9°C
- PSA: 0.00000
- Density: 0.858g/cm3
- LogP: 3.54650
1-TERT-BUTYL-4-ETHYLBENZENE(Cas 7364-19-4) Usage
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General Description |
1-Tert-butyl-4-ethylbenzene is a chemical compound that belongs to the class of organic compounds known as benzene and substituted derivatives. It is a colorless liquid with a faint odor, and is primarily used as a solvent in various industrial applications such as coatings, adhesives, and cleaning products. The chemical structure of 1-tert-butyl-4-ethylbenzene consists of a benzene ring substituted with a tert-butyl group and an ethyl group. It is known to have low toxicity and is relatively stable under normal conditions, but caution should still be taken when handling and storing this chemical to prevent potential health and environmental hazards. |
InChI:InChI=1/C12H18/c1-5-10-6-8-11(9-7-10)12(2,3)4/h6-9H,5H2,1-4H3
7364-19-4 Relevant articles
Chemoselective Hydrogenation of Olefins Using a Nanostructured Nickel Catalyst
Klarner, Mara,Bieger, Sandra,Drechsler, Markus,Kempe, Rhett
supporting information, p. 2157 - 2161 (2021/05/21)
The selective hydrogenation of functiona...
Photo-Initiated Cobalt-Catalyzed Radical Olefin Hydrogenation
Sang, Sier,Unruh, Tobias,Demeshko, Serhiy,Domenianni, Luis I.,van Leest, Nicolaas P.,Marquetand, Philipp,Schneck, Felix,Würtele, Christian,de Zwart, Felix J.,de Bruin, Bas,González, Leticia,V?hringer, Peter,Schneider, Sven
, p. 16978 - 16989 (2021/08/09)
Outer-sphere radical hydrogenation of ol...
Direct Synthesis of Mono-α-arylated Ketones from Alcohols and Olefins via Ni-Catalyzed Oxidative Cross-Coupling
Yang, Peng-Fei,Shu, Wei
supporting information, p. 6203 - 6208 (2020/08/12)
Controlled synthesis of α-monoarylated k...
Generalized Chemoselective Transfer Hydrogenation/Hydrodeuteration
Wang, Yong,Cao, Xinyi,Zhao, Leyao,Pi, Chao,Ji, Jingfei,Cui, Xiuling,Wu, Yangjie
supporting information, p. 4119 - 4129 (2020/08/10)
A generalized, simple and efficient tran...
7364-19-4 Process route
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594-19-4
tert.-butyl lithium
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12203-31-5
(Ethylbenzene)tricarbonylchromium
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-
100-41-4,27536-89-6
ethylbenzene
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14411-56-4
1-(tert-butyl)-3-ethylbenzene
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-
7364-19-4
4-ethyl-tert-butylbenzene
| Conditions | Yield |
|---|---|
|
With
N-Bromosuccinimide;
Yield given. Multistep reaction;
1) THF / -40 deg C / 2h 2) -40 deg C to r.t./ 1h;
|
12 % Chromat.
5 % Chromat. |
|
With
N-Bromosuccinimide;
Yield given. Multistep reaction;
1) THF / -40 deg C / 2h 2) -40 deg C to r.t./ 1h;
|
58 % Chromat.
12 % Chromat. |
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253185-03-4,253185-04-5
tert-butylbenzene
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-
105-58-8,76619-83-5
Diethyl carbonate
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-
100-41-4,27536-89-6
ethylbenzene
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-
105-05-5
1,4-diethylbenzene
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-
1746-23-2,26009-55-2
4-tert-Butylstyrene
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-
7364-19-4
4-ethyl-tert-butylbenzene
| Conditions | Yield |
|---|---|
|
Al-MCM-41;
at 300 ℃;
Further Variations:;
Catalysts;
Temperatures;
Product distribution;
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7364-19-4 Upstream products
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78-83-1
2-methyl-propan-1-ol
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100-41-4
ethylbenzene
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507-19-7
t-butyl bromide
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78-77-3
Isobutyl bromide
7364-19-4 Downstream products
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65276-27-9
2-ethyl-5-tert -butyl-benzyl chloride
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57190-08-6
1-ethyl-2-bromo-4-tert -butyl-benzene
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107342-35-8
2-ethyl-5-tert -butyl-1,3-dinitro-benzene
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100862-89-3
1-(2-ethyl-4-tert -butyl-phenyl)-ethanone