7598-29-0

Basic information

• Product Name: 3-(naphthalen-2-yloxy)propan-1-ol
• CAS NO: 7598-29-0
• Molecular Formula: C₁₃H₁₄O₂
• Molecular Weight: 202.2491
• Mol File: 7598-29-0.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 359.9°C at 760 mmHg
• Flash Point: 166.1°C
• Density: 1.135g/cm³
• Vapor Pressure: 8.32E-06mmHg at 25°C
• Refractive Index: 1.607
• CAS DataBase Reference: 3-(naphthalen-2-yloxy)propan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(naphthalen-2-yloxy)propan-1-ol(7598-29-0)
• EPA Substance Registry System: 3-(naphthalen-2-yloxy)propan-1-ol(7598-29-0)

Safety Data

• Hazardous Substances Data: 7598-29-0(Hazardous Substances Data)

Usage

General Description

3-(naphthalen-2-yloxy)propan-1-ol is a chemical compound that belongs to the class of alcohols. Its chemical structure includes a naphthalene ring, which is a fused double-ring arrangement of carbon atoms, attached to a propanol molecule. 3-(naphthalen-2-yloxy)propan-1-ol is used in organic synthesis and medicinal chemistry as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its properties and applications have not been extensively studied, but it has the potential to be used in the development of new drugs and materials due to the unique structure and reactivity of the naphthalene ring and propanol group. Additionally, the compound may have potential uses in the fields of material science and engineering, due to its ability to modify the physical and chemical properties of polymers and other materials.

Upstream product

• 3245-62-3 2-(3-bromopropoxy)naphthalene 

Downstream Products

• 1414317-08-0 1-[3-(2-naphthoxy)-n-propyl]oxymethyl-4-phenyl-1,2,3-triazole 
• 1414317-14-8 1-methyl-3-((3-(naphthalen-2-yloxy)propoxy)methyl)-5-phenyl-1H-1,2,3-triazol-3-ium trifluoromethanesulfonate 
• 1365252-91-0 C₂₀H₁₉N₃O₄S 
• 1381879-25-9 C₂₉H₃₄N₃O₅S⁽¹⁺⁾*CF₃O₃S^(1-) 
• 1381879-21-5 C₂₈H₃₁N₃O₅S 

Relevant articles and documents

Nucleophilic Hydroxylation in Water Media Promoted by a Hexa-Ethylene Glycol-Bridged Dicationic Ionic Liquid

Hexaethylene glycol bis(3-hexaethylene glycol imidazolium) dimesylate ionic liquid (hexaEG-DHIM) was designed and prepared as a highly efficient promoter for the nucleophilic hydroxylation of alkyl halides to the corresponding alcohol products in neat water media. It was observed that hexaEG-DHIM promoter enhanced the nucleophilicity of water significantly in the reaction. In addition, the hexaEG-DHIM could be reused several times without loss of activity. Moreover, the hydroxylation reactions of base-sensitive and/or polar alkyl halide substrates proceeded highly chemoselectively in excellent yields.