26627-36-1

Basic information

• Product Name: 1,3-Bis(2-propynyloxy)benzene
• Synonyms: 1,3-Bis(2-propynyloxy)benzene
• CAS NO: 26627-36-1
• Molecular Formula: C₁₂H₁₀O₂
• Molecular Weight: 186.2066
• Mol File: 26627-36-1.mol
• Article Data: 34

Chemical Properties

• Melting Point: 38.0 to 42.0 °C
• Appearance: /
• CAS DataBase Reference: 1,3-Bis(2-propynyloxy)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Bis(2-propynyloxy)benzene(26627-36-1)
• EPA Substance Registry System: 1,3-Bis(2-propynyloxy)benzene(26627-36-1)

Safety Data

• Hazardous Substances Data: 26627-36-1(Hazardous Substances Data)

Usage

Description

1,3-Bis(2-propynyloxy)benzene is a chemical compound with the molecular formula C14H12O2. It is a colorless liquid that serves as a monomer in the production of high-performance polymers.

Uses

Used in Polymer Production:
1,3-Bis(2-propynyloxy)benzene is used as a monomer for synthesizing polymeric materials, such as thermosetting resins, which are utilized in the creation of adhesives, coatings, and composites.
Used in Adhesives Industry:
In the adhesives industry, 1,3-Bis(2-propynyloxy)benzene is used as a component in thermosetting resins for its high thermal stability and resistance to chemicals, contributing to the production of durable and long-lasting adhesives.
Used in Coatings Industry:
1,3-Bis(2-propynyloxy)benzene is used as a component in thermosetting resins for coatings, providing high thermal stability and chemical resistance, which are essential for creating long-lasting and durable coatings.
Used in Composites Industry:
In the composites industry, 1,3-Bis(2-propynyloxy)benzene is used as a component in thermosetting resins to enhance the thermal stability and chemical resistance of composite materials, making them suitable for various applications.
Used in Advanced Electronic and Optoelectronic Devices:
1,3-Bis(2-propynyloxy)benzene has potential applications in the development of advanced electronic and optoelectronic devices due to its unique properties, making it a valuable component in the production of specialty polymers for these industries.

Upstream product

• 624-65-7 2-propynyl chloride 
• 108-46-3 recorcinol 
• 3692-88-4 3-hydroxyphenyl propargyl ether 
• 106-96-7 propargyl bromide 

Downstream Products

• 63153-72-0 4-[4-(3-prop-2-ynyloxy-phenoxy)-but-2-ynyl]-morpholine 
• 63153-70-8 1-(4-Dimethylamino-2-butynyloxy)-3-(2-propynyloxy)benzol 
• 63153-71-9 1(4-Diethylamino-2-butynyloxy)-3-(2-propynyloxy)benzol 
• 1402054-00-5 1,3-bis((1-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-1H-1,2,3-triazol-4-yl)methoxy)benzene 
• 1402054-08-3 C₄₀H₅₀N₈O₁₈ 
• 1224691-70-6 4-((3-((1-benzyl-1H-1,2,3-triazol-4-yl)methoxy)phenoxy)methyl)-1-benzyl-1H-1,2,3-triazole 
• 1224691-69-3 C₁₉H₁₇N₃O₂ 
• 312745-14-5 C₆H₄(OCH₂CCAu)2 

Relevant articles and documents

Cholesterol appended bis-1,2,3-triazoles as simple supramolecular gelators for the naked eye detection of Ag+, Cu2+ and Hg2+ ions

Cholesterol coupled bis-1,2,3-triazoles 1-3 have been synthesized and their gelation abilities are examined. Bis triazoles 1-3 form a gel from CHCl3-CH3OH (2: 1, v/v) mixture solvents. In contrast, compounds 4 and 5, which are devoid of triazoles, are unable to form a gel under similar conditions and thus validate the essential role of triazoles in gelation. While the gel phase of 1 detects Cu2+ ions by showing phase transformation from gel to sol, gels derived from 2 and 3 undergo disintegration in the presence of Ag+, Cu2+ and Hg2+ ions. Such phase changes corroborate the visual sensing of metal ions. Moreover, the fluorescence titration of 3 discriminates Cu2+, Hg2+ and Ag+ ions by exhibiting differential quenching.

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THERMOLYSIS-MEDIATED PROCESS FOR MANUFACTURING CHROMENES INTENDED FOR THE PREPARATION OF THERMOSETTING RESINS

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