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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

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

tert.-butyl lithium
594-19-4

tert.-butyl lithium

(Ethylbenzene)tricarbonylchromium
12203-31-5

(Ethylbenzene)tricarbonylchromium

ethylbenzene
100-41-4,27536-89-6

ethylbenzene

1-(tert-butyl)-3-ethylbenzene
14411-56-4

1-(tert-butyl)-3-ethylbenzene

4-ethyl-tert-butylbenzene
7364-19-4

4-ethyl-tert-butylbenzene

Conditions
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.
tert-butylbenzene
253185-03-4,253185-04-5

tert-butylbenzene

Diethyl carbonate
105-58-8,76619-83-5

Diethyl carbonate

ethylbenzene
100-41-4,27536-89-6

ethylbenzene

1,4-diethylbenzene
105-05-5

1,4-diethylbenzene

4-tert-Butylstyrene
1746-23-2,26009-55-2

4-tert-Butylstyrene

4-ethyl-tert-butylbenzene
7364-19-4

4-ethyl-tert-butylbenzene

Conditions
Conditions Yield
Al-MCM-41; at 300 ℃; Further Variations:; Catalysts; Temperatures; Product distribution;

7364-19-4 Upstream products

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    2-methyl-propan-1-ol

  • 100-41-4
    100-41-4

    ethylbenzene

  • 507-19-7
    507-19-7

    t-butyl bromide

  • 78-77-3
    78-77-3

    Isobutyl bromide

7364-19-4 Downstream products

  • 65276-27-9
    65276-27-9

    2-ethyl-5-tert -butyl-benzyl chloride

  • 57190-08-6
    57190-08-6

    1-ethyl-2-bromo-4-tert -butyl-benzene

  • 107342-35-8
    107342-35-8

    2-ethyl-5-tert -butyl-1,3-dinitro-benzene

  • 100862-89-3
    100862-89-3

    1-(2-ethyl-4-tert -butyl-phenyl)-ethanone

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