Catalog |
name |
Description |
price |
R-R-5268 |
4,4,4,4-Silanetetrayltetrabenzaldehyde CAS No.:1055999-34-2 |
4,4,4,4-Silanetetrayltetrabenzaldehyde/CAS No.:1055999-34-2, a versatile chemical compound used in cutting-edge scientific research, offering boundless potential for groundbreaking applications. Explore its fascinating properties and revolutionize your experiments.
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R-R-5269 |
4,4,4,4-([1,1-Biphenyl]-4,4-diylbis(azanetriyl))tetrabenzaldehyde CAS No.:865448-72-2 |
The compound 4,4,4,4-([1,1-Biphenyl]-4,4-diylbis(azanetriyl))tetrabenzaldehyde/CAS No.:865448-72-2 is a complex organic molecule that is likely to have a biphenyl core structure with multiple benzaldehyde groups attached through azanetriyl linkages. This structure suggests potential applications in materials science, organic synthesis, and possibly pharmacology due to the presence of reactive aldehyde groups and the stability provided by the biphenyl moiety.
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R-R-5270 |
[1,1-Biphenyl]-3,3,5,5-tetracarbaldehyde CAS No.:150443-85-9 |
[1,1-Biphenyl]-3,3,5,5-tetracarbaldehyde/CAS No.:150443-85-9 is a versatile chemical compound used in scientific research. Its unique structure allows for diverse applications, ranging from catalysis to materials synthesis, making it a promising tool for advancing various fields of study.
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R-R-5271 |
4,4,4,4-(Pyrene-1,3,6,8-tetrayl)tetrabenzaldehyde CAS No.:1415238-25-3 |
4,4,4,4-(Pyrene-1,3,6,8-tetrayl)tetrabenzaldehyde/CAS No.:1415238-25-3, a chemical compound with diverse applications in scientific research. This compound possesses unique properties that enable its utilization in various fields, including materials science, organic electronics, and optoelectronics. Its conjugated structure and high thermal stability make it an ideal candidate for developing advanced materials and exploring novel technological advancements.
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R-R-5272 |
[1,1:3,1-Terphenyl]-3,3,5,5-tetracarbaldehyde CAS No.:201734-76-1 |
[1,1:3,1-Terphenyl]-3,3,5,5-tetracarbaldehyde/CAS No.:201734-76-1 is a derivative of terphenyls, which are a group of closely related aromatic hydrocarbons. They consist of a central benzene ring substituted with two phenyl groups1.
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R-R-5273 |
Tetrakis(4-formylphenyl)methane CAS No.:617706-61-3 |
Tetrakis(4-formylphenyl)methane/CAS No.:617706-61-3 is a chemical compound used in scientific research. It exhibits high perplexity due to its complex molecular structure, enabling diverse applications in areas like catalysis, material synthesis, and drug development. Its burstiness lies in the versatility it offers, making it a promising candidate for innovative scientific advancements.
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R-R-5302 |
4,4,4,4-(Ethene-1,1,2,2-tetrayl)tetrakis(N,N-diphenyl-[1,1-biphenyl]-4-amine)/CAS No.:1416786-56-5 |
4,4,4,4-(Ethene-1,1,2,2-tetrayl)tetrakis(N,N-diphenyl-[1,1-biphenyl]-4-amine)/CAS No.:1416786-56-5 from ruixi.This compound features a tetraphenylethylene core with four terminal aldehyde groups . It is extensively used as an organic linker for synthesizing covalent organic frameworks (COFs) .
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R-R-5316 |
4-{2,2-Bis[(4-formylphenoxy)methyl]-3-(4-formylphenoxy)propoxy}benzaldehyde CAS No.:381670-43-5 |
4-{2,2-Bis[(4-formylphenoxy)methyl]-3-(4-formylphenoxy)propoxy}benzaldehyde/CAS No.:381670-43-5 is a chemical compound with the molecular formula C33H28O8 and a molecular weight of 552.57 . It is used as a monomer to synthesize COF materials .
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R-R-5330 |
1,3,5-Tris[4-(hydroxysulfonyl)phenyl]benzene CAS No.:343821-13-6 |
1,3,5-Tris(4-hydroxyphenyl)benzene/CAS No.:343821-13-6 is a compound composed of three hydroxyphenyl groups attached to a benzene ring . It is a type of aromatic compound that can be used in the formation of covalent aromatic frameworks (COF) .
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R-R-5453 |
4,4,4-Nitrilotris(([1,1-biphenyl]-4-carboxylic acid)) CAS No.:1239602-35-7 |
4,4,4-Nitrilotris(([1,1-biphenyl]-4-carboxylic acid))/CAS No.:1239602-35-7, also known as 4,4,4-Nitrilotribenzoic acid , is a chemical compound with the molecular formula C21H15NO6 . It has a triangular structure with a triarylamine core and three aldehyde functional groups . The triarylamine core is electron rich, and the aldehyde groups condense with amines to form imine linkages in covalent organic frameworks (COFs) .
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