orophenoxy)phenyL

orophenoxy)phenyL - Names and Identifiers

Name	2-(4-Chloro-phenoxy)-Phenylacetic Acid
Synonyms	orophenoxy)phenyL 2-(4-Chlorophenoxy)phenylacetic acid 2-(4-chlorophenoxy)Benzeneacetic acid 2-(4-Chloro-phenoxy)-Phenylacetic Acid 2-(2-(4-chlorophenoxy)phenyl)acetic acid Benzeneacetic acid, 2-(4-chlorophenoxy)-
CAS	25563-04-6

orophenoxy)phenyL - Physico-chemical Properties

Molecular Formula	C14H11ClO3
Molar Mass	262.69
Density	1.317
Melting Point	120-122℃
Boling Point	397.7±27.0 °C(Predicted)
Solubility	Chloroform (Slightly), Methanol (Slightly, Sonicated)
Appearance	Solid
Color	Light Pinkish-Beige
pKa	4.10±0.10(Predicted)
Storage Condition	Sealed in dry,Room Temperature
Use	This product is for scientific research only and shall not be used for other purposes.

orophenoxy)phenyL - Introduction

2-(4-chroo-phenoxy)-Phenylacetic Acid is an organic compound with the chemical formula C14H11ClO3. The following is a description of its nature, use, formulation and safety information:

Nature:
-Appearance: White crystal powder
-Solubility: Soluble in organic solvents such as ethanol and acetone, insoluble in water
-Melting point: about 130-132 ° C
-Molecular weight: about 266.69g/mol

Use:
2-(4-chroo-phenoxy)-Phenylacetic Acid has certain biological activity and is often used as an important raw material in the synthesis of pharmaceutical intermediates and pesticides. It is also used in the synthesis of organic synthetic reagents, ligands, dyes, etc.

Method:
The preparation method of 2-(4-chloroo-phenoxy)-Phenylacetic Acid can be obtained by the following reaction:
1. P-chlorophenol and bromobenzene are reacted under alkaline conditions to obtain (4-chlorophenyl) benzene alcohol.
2. React (4-chlorophenyl) benzene with bromoacetate to generate 2-(4-Chloro-phenoxy)-Phenylacetic Acid ethyl ester.
3. Finally, 2-(4-chloroo-phenoxy)-Phenylacetic Acid ethyl ester is hydrolyzed by Acid or alkali to obtain the target product.

Safety Information:
2-(4-chloroo-phenoxy)-Phenylacetic Acid is generally relatively safe under normal conditions of use. However, as a chemical, it still needs to be handled and preserved properly.
-Contact: Avoid direct skin contact and prevent inhalation or ingestion.
-fire Source: avoid contact with open flame, to prevent the production of combustible gas.
-Storage: Store in a sealed container, away from fire and oxidizing agents, and avoid direct sunlight.
-Waste Disposal: Disposal in accordance with local regulations.

Last Update：2024-04-09 21:00:56