949015-02-5

Basic information

• Product Name: 1,3-Dioxolan-2-one, 4-[(2-propyn-1-yloxy)methyl]-
• Synonyms: 1,3-Dioxolan-2-one, 4-[(2-propyn-1-yloxy)methyl]-
• CAS NO: 949015-02-5
• Molecular Formula: C₇H₈O₄
• Molecular Weight: 0
• Mol File: 949015-02-5.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,3-Dioxolan-2-one, 4-[(2-propyn-1-yloxy)methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dioxolan-2-one, 4-[(2-propyn-1-yloxy)methyl]-(949015-02-5)
• EPA Substance Registry System: 1,3-Dioxolan-2-one, 4-[(2-propyn-1-yloxy)methyl]-(949015-02-5)

Safety Data

• Hazardous Substances Data: 949015-02-5(Hazardous Substances Data)

Usage

General Description

1,3-Dioxolan-2-one, 4-[(2-propyn-1-yloxy)methyl]- is a chemical compound that is used in various industrial applications. It is a cyclic organic compound with a dioxolane ring and a propynyl functional group. This chemical can be used as a solvent in the production of polymers and resins, as well as in the synthesis of pharmaceuticals and agrochemicals. It is also utilized as a building block in the creation of various specialty chemicals and materials. Overall, 1,3-Dioxolan-2-one, 4-[(2-propyn-1-yloxy)methyl]- plays a crucial role in a wide range of industrial processes and product formulations.

Upstream product

• 124-38-9 carbon dioxide 
• 13580-38-6 3-(prop-2-yn-1-yloxy)propan-1,2-diol 
• 115-19-5 2-methyl-but-3-yn-2-ol 

Downstream Products

• 119-61-9 benzophenone 
• 76-84-6 triphenylmethyl alcohol 
• 92-52-4 biphenyl 
• 597-49-9 3-ethylpentan-3-ol 

Relevant articles and documents

Highly regio- And stereoselective synthesis of cyclic carbonates from biomass-derived polyols: Via organocatalytic cascade reaction

The cascade reaction of CO2, vicinal diols, and propargylic alcohol, was firstly achieved by dual Lewis base (LB) organocatalytic systems involving LB-CO2 adducts and commercially available organic amines. This methodology could overcome the chemical inertness of CO2, providing an alternative route to various functionalized five-membered cyclic carbonates in moderate to high yields under mild reaction conditions (25 °C, 1.0 atm of CO2). More importantly, this method could also be applied for facile and efficient synthesis of chiral polycyclic carbonates from biomass-derived polyols with complete configuration retention of chiral centers. This study provides an environment-friendly, scalable and cost effective protocol to construct value-added cyclic carbonates with multi-functional groups and chiral centers.