726-44-3

Basic information

• Product Name: 1,3-diphenoxypropane
• Synonyms: Trimethylenebis(phenyl ether);3-phenoxypropoxybenzene;1,3-diphenoxypropane
• CAS NO: 726-44-3
• Molecular Formula: C₁₅H₁₆O₂
• Molecular Weight: 228.289
• Mol File: 726-44-3.mol
• Article Data: 5

Chemical Properties

• Melting Point: 62°C
• Boiling Point: 339°C (estimate)
• Flash Point: 132.5°C
• Appearance: /
• Density: 1.0657 (rough estimate)
• Refractive Index: 1.5542 (estimate)
• CAS DataBase Reference: 1,3-diphenoxypropane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-diphenoxypropane(726-44-3)
• EPA Substance Registry System: 1,3-diphenoxypropane(726-44-3)

Safety Data

• Hazardous Substances Data: 726-44-3(Hazardous Substances Data)

Usage

General Description

1,3-diphenoxypropane, also known as diphenyl ether, is a chemical compound with the molecular formula C15H14O2. It is a colorless liquid with a mild, floral odor, and it is commonly used as a solvent in various industrial applications, such as in the manufacturing of dyes, perfumes, and pharmaceuticals. It is also used as a heat transfer fluid, and as a component in the production of some types of plastics and resins. Additionally, 1,3-diphenoxypropane has insecticidal properties and is sometimes used as an insecticide. However, it is important to handle this chemical with care, as it can be harmful if ingested, inhaled, or absorbed through the skin.

Upstream product

• 627-31-6 1,3-Diiodopropane 
• 139-02-6 sodium phenoxide 
• 6180-61-6 3-phenoxypropanol 
• 88284-48-4 2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 142-28-9 1,3-Dichloropropane 
• 108-95-2 phenol 
• 5469-66-9 propane-1,3-diol ditosylate 
• 109-64-8 1,3-dibromo-propane 

Downstream Products

• 52206-77-6 1,3-bis[4-(alpha-aminobenzyl)phenoxy]propane 
• 52206-97-0 1,3-Bis(4-benzoylphenoxy)propane dioxime 
• 52224-46-1 1,3-bis(4-benzoylphenoxy)propane 
• 855926-42-0 4,4-[1,3-propanediylbis(oxy)]bisbenzeneacetonitrile 
• 3722-80-3 1,3-bis(4-formylphenoxy)propane 

Relevant articles and documents

Prospective new amidinothiazoles as leukotriene B4 inhibitors

An efficient and one-step synthesis of the versatile, hitherto new derivatives resembling LY293111, a prospective potent antagonist of the leukotriene B4 (LTB4) receptor, were reported. The strategy was based on the synthesis of an amidinothiazole ring, c

Structure-property correlations in model compounds of oligomer liquid crystals

Structure-property correlations of the following model compounds for oligomer liquid crystals (LCs) have been investigated: monomers, C 6H5O(CH2)xCH3 (x = 4 and 5); dimers, C6H5O

SYNTHETIC APPLICATION OF MICELLAR CATALYSIS. WILLIAMSON'S SYNTHESIS OF ETHERS

A simple, rapid and efficient procedure for the preparation of di-alkyl, simple phenyl-alkyl and hindered phenyl-alkyl ethers has been developed.Based on the principle of micellar catalysis the method involves alkylation of the alkoxide or the phenoxide ion with an alkyl chloride at 80 deg C in the presence of cationic micelles.For the preparation of phenyl-alkyl ethers normal micelles were used, while for the di-alkyl ethers reverse micelles were more effective.By increasing the ionic strength of the solution the rate of formation of phenyl-alkyl ethers could be increased.