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4-Ethylbenzyl chloride

  • CAS No.: 1467-05-6
  • Purity: 99%
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Cost-effective and customizable 4-Ethylbenzyl chloride 1467-05-6 in stock

  • Molecular Formula: C9H11Cl
  • Molecular Weight: 154.639
  • Vapor Pressure: 0.198mmHg at 25°C 
  • Melting Point: -21°C 
  • Refractive Index: 1.5320 
  • Boiling Point: 217.1 °C at 760 mmHg 
  • Flash Point: 83.5 °C 
  • PSA: 0.00000 
  • Density: 1.031 g/cm3 
  • LogP: 2.98780 

4-Ethylbenzyl chloride(Cas 1467-05-6) Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 68, p. 1670, 1946 DOI: 10.1021/ja01212a513

InChI:InChI=1/C9H11Cl/c1-2-8-3-5-9(7-10)6-4-8/h3-6H,2,7H2,1H3

1467-05-6 Relevant articles

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Kosolapoff

, p. 1670 (1946)

-

Efficient selective synthesis of ethylbenzonitriles

Xie, Guangyong,Zhang, Aiqing

, p. 375 - 379 (2012)

Ethylbenzonitriles were synthesized by s...

Cu(II)/Cu(0)@UiO-66-NH2: Base metal@MOFs as heterogeneous catalysts for olefin oxidation and reduction

Wang, Jian-Cheng,Hu, Yu-Hong,Chen, Gong-Jun,Dong, Yu-Bin

, p. 13116 - 13119 (2016)

Two copper-loaded MOF materials, namely ...

Structure-guided optimization of 1H-imidazole-2-carboxylic acid derivatives affording potent VIM-Type metallo-β-lactamase inhibitors

Yan, Yu-Hang,Li, Wenfang,Chen, Wei,Li, Chao,Zhu, Kai-Rong,Deng, Ji,Dai, Qing-Qing,Yang, Ling-Ling,Wang, Zhenling,Li, Guo-Bo

, (2021/11/17)

Production of metallo-β-lactamases (MBLs...

Preparation method of 4-ethylbenzyl chloride

-

Paragraph 0027-0029, (2021/11/26)

The invention discloses a preparation me...

An efficient and convenient chloromethylation of some aromatic compounds catalyzed by zinc iodide

Tang, Jian,Liu, Hongtao,Zhou, Jing,Zhang, Xingxian

, p. 34 - 38 (2019/06/21)

Treatment of a series of aromatic hydroc...

A practical and convenient Blanc-type chloromethylation catalyzed by zinc chloride under solvent-free conditions

Tang, Jian,Liu, Hongtao,He, Kailun,Zhang, Xingxian

, p. 925 - 932 (2019/03/17)

Chloromethylation of various aromatic hy...

1467-05-6 Process route

Dimethoxymethane
109-87-5

Dimethoxymethane

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

ethylbenzene

4-ethylbenzylchloride
1467-05-6

4-ethylbenzylchloride

Conditions
Conditions Yield
Dimethoxymethane; With chlorosulfonic acid; zinc(II) iodide; In dichloromethane; at -10 ℃; for 0.5h;
ethylbenzene; In dichloromethane; at 5 - 10 ℃; for 1h;
87%
Dimethoxymethane; With chlorosulfonic acid; zinc(II) chloride; at -10 ℃; for 0.5h;
ethylbenzene; at 5 - 10 ℃; for 3h;
77%
formaldehyde diethyl acetal
462-95-3

formaldehyde diethyl acetal

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

ethylbenzene

4-ethylbenzylchloride
1467-05-6

4-ethylbenzylchloride

Conditions
Conditions Yield
formaldehyde diethyl acetal; With chlorosulfonic acid; tris(pentafluorophenyl)borate; In dichloromethane; at -5 ℃; for 0.5h; Inert atmosphere;
ethylbenzene; In dichloromethane; at -5 - 0 ℃; for 1h; Inert atmosphere;
85.7%

1467-05-6 Upstream products

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    formaldehyd

  • 100-41-4
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    ethylbenzene

  • 768-59-2
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    4-ethylbenzyl alcohol

  • 107-30-2
    107-30-2

    chloromethyl methyl ether

1467-05-6 Downstream products

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    861318-10-7

    (4-ethyl-benzyl)-methyl-(4-methyl-benzyl)-amine

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    diethyl 4-ethylbenzylmalonate

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    51632-28-1

    (4-ethyl-phenyl)-acetonitrile

  • 67035-84-1
    67035-84-1

    p-ethylbenzyl acetate

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