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4-ETHYLPHENOXYACETIC ACID

  • Chemical Name: 4-ETHYLPHENOXYACETIC ACID
  • CAS: 24431-27-4
  • Purity: 99%
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Manufacturer supply good quality 4-ETHYLPHENOXYACETIC ACID 24431-27-4 with stock

  • Molecular Formula: C10H12 O3
  • Molecular Weight: 180.203
  • Vapor Pressure: 0.000272mmHg at 25°C 
  • Melting Point: 92-94°C 
  • Boiling Point: 309.6°Cat760mmHg 
  • Flash Point: 121.6°C 
  • PSA: 46.53000 
  • Density: 1.144g/cm3 
  • LogP: 1.71240 

4-ETHYLPHENOXYACETIC ACID(Cas 24431-27-4) Usage

General Description

4-Ethylphenoxyacetic acid is a chemical compound that is often used in the synthesis of pharmaceuticals and other organic compounds. It has the molecular formula C10H12O3. 4-ETHYLPHENOXYACETIC ACID is an aromatic ether and it belongs to the class of organic compounds known as phenylpropanoic acids. Its synthesis involves the reaction of 4-ethylphenol with chloroacetic acid in the presence of a base. In terms of its properties, it can appear as a pale yellow to yellow liquid and has a fruit-like odor. Safety measures should be taken while handling it as it may cause irritation to the eyes, skin, and respiratory tract.

InChI:InChI=1/C10H12O3/c1-2-8-3-5-9(6-4-8)13-7-10(11)12/h3-6H,2,7H2,1H3,(H,11,12)

24431-27-4 Relevant articles

ROLES OF MODULATORS OF INTERSECTIN-CDC42 SIGNALING IN ALZHEIMER'S DISEASE

-

Paragraph 0272; 0275; 0277, (2019/04/14)

Methods of treating Alzheimer's disease ...

Methyl 3-(3-(4-(2,4,4-Trimethylpentan-2-yl)phenoxy)-propanamido)benzoate as a Novel and Dual Malate Dehydrogenase (MDH) 1/2 Inhibitor Targeting Cancer Metabolism

Naik, Ravi,Ban, Hyun Seung,Jang, Kyusic,Kim, Inhyub,Xu, Xuezhen,Harmalkar, Dipesh,Shin, Seong-Ah,Kim, Minkyoung,Kim, Bo-Kyung,Park, Jaehyung,Ku, Bonsu,Oh, Sujin,Won, Misun,Lee, Kyeong

, p. 8631 - 8646 (2017/11/03)

Previously, we reported a hypoxia-induci...

Finding new elicitors that induce resistance in rice to the white-backed planthopper Sogatella furcifera

He, Xingrui,Yu, Zhaonan,Jiang, Shaojie,Zhang, Peizhi,Shang, Zhicai,Lou, Yonggen,Wu, Jun

supporting information, p. 5601 - 5603 (2015/11/17)

Herein we report a new way to identify c...

Oxadiazole-isopropylamides as potent and noncovalent proteasome inhibitors

Ozcan, Sevil,Kazi, Aslamuzzaman,Marsilio, Frank,Fang, Bin,Guida, Wayne C.,Koomen, John,Lawrence, Harshani R.,Sebti, Sa?d M.

supporting information, p. 3783 - 3805 (2013/06/27)

Screening of the 50 000 ChemBridge compo...

24431-27-4 Process route

ethyl 2-(4-ethylphenoxy)acetate
71475-45-1

ethyl 2-(4-ethylphenoxy)acetate

2-(4-ethylphenoxy)acetic acid
24431-27-4

2-(4-ethylphenoxy)acetic acid

Conditions
Conditions Yield
ethyl 2-(4-ethylphenoxy)acetate; With sodium hydroxide; In tetrahydrofuran; for 2h; Reflux;
With hydrogenchloride; In water; pH=1;
91%
With potassium hydroxide;
With sodium hydroxide; Heating;
With water; lithium hydroxide; In tetrahydrofuran;
With water; lithium hydroxide;
C<sub>10</sub>H<sub>11</sub>O<sub>3</sub><sup>(1-)</sup>*Na<sup>(1+)</sup>

C10 H11 O3 (1-) *Na(1+)

2-(4-ethylphenoxy)acetic acid
24431-27-4

2-(4-ethylphenoxy)acetic acid

Conditions
Conditions Yield
With hydrogenchloride; In water; pH=1;

24431-27-4 Upstream products

  • 123-07-9
    123-07-9

    4-Ethylphenol

  • 79-11-8
    79-11-8

    chloroacetic acid

  • 71475-45-1
    71475-45-1

    ethyl 2-(4-ethylphenoxy)acetate

  • 79-08-3
    79-08-3

    bromoacetic acid

24431-27-4 Downstream products

  • 71475-47-3
    71475-47-3

    N-(3-Diethylamino-propyl)-2-(4-ethyl-phenoxy)-acetamide

  • 76964-16-4
    76964-16-4

    N-(4-Methyl-3-pentenyl)-p-ethylphenoxyacetamide

  • 84457-75-0
    84457-75-0

    2-(4-Ethyl-phenoxy)-N-(3-isopropoxy-propyl)-acetamide

  • 123-07-9
    123-07-9

    4-Ethylphenol

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