Catalog |
name |
Description |
price |
R-R-5168 |
6,13-Bis(triisopropylsilylethynyl)pentacene CAS No.:373596-08-8 |
6,13-Bis(triisopropylsilylethynyl)pentacene/CAS No.:373596-08-8 is a molecule that has garnered significant attention due to its role as a prototypical organic semiconductor and its potential applications in photovoltaic materials. Its electrochemical properties are of particular interest, as they are crucial for its function in electronic devices .
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R-R-5169 |
4,4-Diethynylbiphenyl CAS No.:38215-38-2 |
4,4-Diethynylbiphenyl/CAS No.:38215-38-2 is a chemical compound that serves as a monomer or comonomer in the synthesis of various polymeric materials. It is characterized by the presence of two ethynyl groups attached to a biphenyl structure, which allows it to participate in polymerization reactions to form extended conjugated networks. These networks can exhibit a range of properties depending on the specific synthesis and functionalization methods employed .
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R-R-5170 |
1,5-Bis(trimethylsilyl)penta-1,4-diyn-3-one CAS No.:60836-10-4 |
1,5-Bis(trimethylsilyl)penta-1,4-diyn-3-one (BTSPD)/CAS No.:60836-10-4 is an organic compound that belongs to the class of diynes. Diynes are organic compounds that contain two triple bonds separated by a chain of atoms. The molecular formula of BTSPD is C11H18OSi2.
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R-R-5171 |
9,10-Di(trimethylsilylethynyl)anthracene CAS No.:18750-95-3 |
9,10-Di(trimethylsilylethynyl)anthracene (DTEA)/CAS No.:18750-95-3 is a highly conjugated organic compound that is widely used in materials science and industry. It is a novel organic photocatalyst .
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R-R-5172 |
1,3,5-Triethynylbenzene CAS No.:7567-63-7 |
1,3,5-Triethynylbenzene/CAS No.:7567-63-7 is a multifunctional organic compound that serves as a building block in various chemical syntheses. It is characterized by the presence of three ethynyl groups attached to a benzene ring at the 1, 3, and 5 positions. This arrangement allows for a high degree of reactivity and the potential to form complex molecular architectures, including dendrimers and star-shaped polymers.
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R-R-5173 |
1,3,5-Tris(4-ethynylphenyl)benzene CAS No.:71866-86-9 |
1,3,5-Tris(4-ethynylphenyl)benzene/CAS No.:71866-86-9 is a complex chemical compound with diverse applications in scientific research. Its unique structure allows for the development of advanced materials, catalysts, and electronic devices, opening doors to groundbreaking discoveries.
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R-R-5174 |
Tris(4-ethynylphenyl)amine CAS No.:189178-09-4 |
Tris(4-ethynylphenyl)amine/CAS No.:189178-09-4, also known as tris(4-ethynylphenyl)amine, is an aromatic organic compound with three ethynyl groups attached to a phenyl ring. It is used in a variety of applications, including organic synthesis, pharmaceuticals, and materials science. It is also used as an intermediate in the synthesis of other compounds.
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R-R-5175 |
Tetrakis(4-ethynylphenyl)ethene CAS No.:4863-90-5 |
Tetrakis(4-ethynylphenyl)ethene/CAS No.:4863-90-5 is a compound with the molecular formula C34H20 . It has a molecular weight of 428.5 g/mol . The compound is also known by other names such as 1,1,2,2-Tetrakis(4-ethynylphenyl)ethene and 1-ethynyl-4-[1,2,2-tris(4-ethynylphenyl)ethenyl]benzene .
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R-R-5176 |
Hexakis[(trimethylsilyl)ethynyl]benzene CAS No.:100516-62-9 |
Hexakis[(trimethylsilyl)ethynyl]benzene/HEB-TMS/CAS No.:100516-62-9 is a starting monomer for synthesizing Graphdiyne (GDY), an emerging carbon allotrope . The synthesis of GDY involves a cross-coupling reaction on the surface of copper foil . A deprotection-free method has also been developed to grow GDY on the surface of C3N4 by directly using HEB-TMS as the precursor .
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R-R-5177 |
1,2,4,5-Tetraethynylbenzene CAS No.:70603-31-5 |
1,2,4,5-Tetraethynylbenzene (TEB)/CAS No.:70603-31-5 is a small organic molecule that is part of a larger class of molecules known as polycyclic aromatic hydrocarbons (PAHs). TEB is a planar molecule with a structure consisting of four ethynyl groups attached to a benzene ring. TEB has been used in a variety of scientific research applications due to its unique properties and its ability to form covalent bonds with other molecules. TEB has been studied for its potential use in organic synthesis, as a catalyst in chemical reactions, and as a fluorescent dye.
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