54373-15-8

Basic information

• Product Name: 4-(2-CHLOROETHOXY)BENZALDEHYDE
• Synonyms: P-(2-CHLOROETHOXY)BENZALDEHYDE;4-(2-CHLOROETHOXY)BENZALDEHYDE
• CAS NO: 54373-15-8
• Molecular Formula: C₉H₉ClO₂
• Molecular Weight: 184.62
• Product Categories: Aldehydes;blocks
• Mol File: 54373-15-8.mol
• Article Data: 14

Chemical Properties

• Melting Point: 25-30°C
• Boiling Point: 308.6 °C at 760 mmHg
• Flash Point: 137.6 °C
• Appearance: /
• Density: 1.206 g/cm³
• Vapor Pressure: 0.000673mmHg at 25°C
• Refractive Index: 1.555
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: 4-(2-CHLOROETHOXY)BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2-CHLOROETHOXY)BENZALDEHYDE(54373-15-8)
• EPA Substance Registry System: 4-(2-CHLOROETHOXY)BENZALDEHYDE(54373-15-8)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 54373-15-8(Hazardous Substances Data)

Usage

General Description

4-(2-chloroethoxy)benzaldehyde is an organic compound with the chemical formula C9H9ClO2. It is a colorless to light yellow liquid with a strong, sweet, and floral odor. 4-(2-CHLOROETHOXY)BENZALDEHYDE is commonly used as an intermediate in the synthesis of various pharmaceuticals, pesticides, and other organic compounds. It can also be used as a flavor and fragrance ingredient in the production of perfumes and other personal care products. 4-(2-chloroethoxy)benzaldehyde is a versatile chemical that plays an important role in the production of a wide range of consumer and industrial products.

InChI:InChI=1/C9H9ClO2/c10-5-6-12-9-3-1-8(7-11)2-4-9/h1-4,7H,5-6H2

Upstream product

• 123-08-0 4-hydroxy-benzaldehyde 
• 107-04-0 1-Bromo-2-chloroethane 
• 80-41-1 2-chloroethyl tosylate 
• 624-70-4 1-chloro-2-iodoethane 
• 107-06-2 1,2-dichloro-ethane 
• 104-88-1 4-chlorobenzaldehyde 

Downstream Products

• 82625-33-0 (Z)-3-[4-(2-Chloro-ethoxy)-phenyl]-2-(5-methoxy-benzo[d]isoxazol-3-yl)-acrylonitrile 
• 919992-12-4 2-[4-(2-chloroethoxy)phenyl]-[1,3]dithiane 
• 142649-91-0 4-[2-(2(3H)-benzoxazolon-3-yl)ethoxy]benzaldehyde 
• 242478-04-2 2-[4-(2-chloro-ethoxy)-phenyl]-8-methoxy-3-(4-methoxy-phenyl)-2,3-dihydro-1H-quinazolin-4-one 
• 205371-43-3 4-[2-(1H-imidazole-1-yl)ethoxy]benzaldehyde 
• 836595-50-7 methyl 3-[4-(2-chloroethoxy)phenyl]-2-ethoxy-2-propenoate 
• 34074-28-7 1,2-bis(4-formylphenoxy)ethane 
• 1446339-59-8 (S)-3-{1-[2-(4-formylphenoxy)ethyl]piperidin-2-yl}pyridine oxalate 
• 1616111-02-4 (Z)-2-{4-[2-(4-methylpiperazin-1-yl)ethoxy]-benzylidene}-3-oxo-2,3-dihydrobenzofuran-7-carboxamide 
• 26815-04-3 4-(2-(piperidin-1-yl)ethoxy)benzaldehyde 
• 82625-45-4 4-(2-morpholin-4-yl-ethoxy)-benzaldehyde 
• 15182-94-2 4-[2-(diethylamino)ethoxy]benzaldehyde 
• 15182-92-0 4-(2-dimethylaminoethoxy)benzaldehyde 
• 100238-55-9 4-(2-chloroethoxy)phenol 

Relevant articles and documents

Effect of 6-Benzoyl-benzothiazol-2-one scaffold on the pharmacological profile of α-alkoxyphenylpropionic acid derived PPAR agonists

A series of nitrogen heterocycles containing α–ethoxyphenylpropionic acid derivatives were designed as dual PPARα/γ agonist ligands for the treatment of type 2 diabetes (T2D) and its complications. 6-Benzoyl-benzothiazol-2-one was the most tolerant of the

USE OF DISUBSTITUTED BENZENES TO CONTROL INSECTICIDE-RESISTANT PESTS

The invention is in the technical field of insect control and relates to the use of a disubstituted benzenes for controlling insecticide-resistant pests such as mosquitoes and cockroaches.

Anti-diabetic activity of fused PPARγ-SIRT1 ligands with limited body-weight gain by mimicking calorie restriction and decreasing SGK1 expression

A series of benzothiazol-2-one containing α-ethoxyphenylpropionic acid derivatives incorporating resveratrol or butein scaffolds were designed as fused full PPARγ agonist ligands and SIRT1-activating compounds for the treatment of type 2 diabetes (T2D) an