Propargyl ether
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Category | Bis-propargyl-PEGn |
Catalog NO. | BPG-3569 |
Product Name | Propargyl ether |
CAS | 6921-27-3 |
Molecular Formula | C6H6O |
Molecular Weight | 94.11 |
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Description | Propargyl ether is a homobifunctional PEG linker with two propargyl groups. The propargyl group forms triazole linkage with azide-bearing compounds or biomolecules via copper catalyzed Click Chemistry. |
Synonyms | 3-(prop-2-yn-1-yloxy)prop-1-yne; Dipropargyl ether; Bis-propargyl-PEG1; 1-Propyne, 3,3'-oxybis-; Bispropargyl ether; Di(2-propynyl) ether; Bis(2-propynyl) ether; 3-(2-Propynyloxy)-1-propyne |
IUPAC Name | 3-prop-2-ynoxyprop-1-yne |
Canonical SMILES | C#CCOCC#C |
InChI | InChI=1S/C6H6O/c1-3-5-7-6-4-2/h1-2H,5-6H2 |
InChIKey | HRDCVMSNCBAMAM-UHFFFAOYSA-N |
Boiling Point | 55-57°C at 65 mmHg |
Purity | ≥95% |
Density | 0.914 g/mL at 25°C |
Appearance | Pale Yellow or Colorless Oily Liquid |
Storage | Store at 2-8°C |
Exact Mass | 94.041864811 |
LogP | 0.26940 |
Pictogram(s) | Flammable, Irritant |
Signal | Warning |
Precautionary Statement Codes | P210, P233, P240, P241, P242, P243, P264, P270, P280, P301+P317, P303+P361+P353, P330, P370+P378, P403+P235, and P501 |
Propargyl ether, an organic compound with diverse industrial and research applications, offers a multitude of utilization possibilities. Here are four key applications of propargyl ether, described with elevated perplexity and burstiness: Polymer Chemistry: At the forefront of polymer innovation, propargyl ether plays a pivotal role as both a monomer and a cross-linking agent in the synthesis of advanced polymeric materials. Its unique alkyne functional group unlocks the potential for crafting highly versatile polymers endowed with superior thermal and mechanical properties. This attribute makes it a cornerstone in applications necessitating resilient and robust materials such as coatings, adhesives, and composites. Pharmaceutical Synthesis: Within the realm of pharmaceuticals, propargyl ether emerges as a fundamental building block essential for synthesizing complex molecular frameworks vital for drug development. Its inherent reactivity enables the construction of intricate molecules crucial for the creation of novel pharmaceuticals. Propargyl ether derivatives find significant utility in click chemistry, a method facilitating the rapid and effective assembly of biologically active compounds, propelling pharmaceutical innovation forward. Agricultural Chemical Development: In the realm of agrochemicals, propargyl ether showcases its prowess in the synthesis of pesticides and herbicides tailored for precision targeting of pest populations while safeguarding crop health. Its chemical properties empower the creation of compounds capable of selectively controlling pests without causing harm to crops, ensuring minimal environmental impact while bolstering agricultural productivity sustainably. Material Science Research: In the dynamic field of material science, propargyl ether shines as a key component in developing functional materials boasting unique properties. Its versatile nature enables the synthesis of materials with heightened conductivity, offering significant value in the production of cutting-edge electronic devices. Furthermore, its capacity to generate self-healing polymers sparks exploration into applications in smart materials and coatings, pushing the boundaries of material science innovation. |
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