Tri-aryl compounds/what is this

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In summary, the aryl group refers to an aromatic group having at least one carbocyclic aromatic group or heterocyclic aromatic group, which may be unsubstituted or substituted by one or more groups selected from halogen, haloalkyl, hydroxy, alkoxy, carbonyl, amido, alkylamido, dialkylamido, nitro, cyano, amino, monoalkylamino, dialkylamino, carboxy or thio or thioalkyl. The aryl group is between 4-12 membered ring(s). The aryl group is between 6-18 membered ring(s). The aryl group is between 4
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  • #2
Ri is nothing, alkoxy, OCH2COOEt or halogen

R2 and R3 are independently hydrogen, alkyl, alkoxy, hydroxyl, or OCH2COOAIk; and

R4 and R5 are hydrogens or form together a saturated or unsaturated of 5-7 carbocyclic ring; or- its isomer, salt, hydrate, N-oxide, crystal or any combination thereof; and a carrier, diluents, or any combination thereof
 
  • #3
proculation? says rubbish.

Aryl is one benzene ring attached to something with one covalent bond (called phenyl alcohol= phenol), biaryl- is 2, triaryl- is 3, etc.
These aromatic rings can be fused rings...anthracene has fused rings
 
  • #4
The patent defines the aryl group as:

[0048] An "aryl" group refers, in another embodiment, to an aromatic group having at least one carbocyclic aromatic group or heterocyclic aromatic group, which may be unsubstituted or substituted by one or more groups selected from halogen, haloalkyl, hydroxy, alkoxy, carbonyl, amido, alkylamido, dialkylamido, nitro, cyano, amino, monoalkylamino, dialkylamino, carboxy or thio or thioalkyl. In another embodiment, the aryl group is between 4-12 membered ring(s). In another embodiment, the aryl group is between 6-18 membered ring(s). In another embodiment, the aryl group is between 4-8 membered ring(s). In another embodiment, the aryl group is a 6 membered ring. In another embodiment, the aryl group is a fused ring system comprising of between 2-3 rings. Nonlimiting examples of aryl rings are phenyl, naphthyl, pyranyl, pyrrolyl, pyrazinyl, pyrimidinyl, pyrazolyl, pyridinyl, furanyl, thiophenyl, thiazolyl, imidazolyl, isoxazolyl, and the like.

In this patent application the structure is shown in the orginal document but not in this on line summary. To wit:

006] In one embodiment, this invention provides a compound represented by the structure represented by formula I:


wherein... etc...

You probably have to pay to play, eh?
 
  • #5


Tri-aryl compounds refer to molecules that contain three aryl groups, which are aromatic rings with at least one substituent. These compounds have a variety of potential applications in fields such as pharmaceuticals, materials science, and organic electronics.

The links provided do not specify the exact tri-aryl compounds being discussed, but rather provide patent information for a specific group of tri-aryl compounds and their potential uses. It is possible that the actual compounds are listed in the patent documents, but without further information it is not possible to determine the specific compounds being referred to. It is also important to note that these compounds may have different names or structures depending on the specific substituents attached to the aryl groups. Further research or consultation with a chemist may be necessary to determine the exact compounds being referenced.
 
  • #6


Tri-aryl compounds are a class of chemical compounds that contain three aryl groups bonded to a central carbon atom. These compounds have various applications in the fields of organic synthesis, medicinal chemistry, and materials science. The pages provided do not list specific tri-aryl compounds, but rather describe the general structure and potential uses of this class of compounds. Additional research would be needed to determine the exact compounds mentioned in these pages.
 

What are tri-aryl compounds?

Tri-aryl compounds are molecules that contain three aromatic rings, with each ring connected to at least one other ring through a carbon-carbon bond. These compounds are often used in pharmaceuticals, agrochemicals, and materials science due to their unique properties.

How are tri-aryl compounds synthesized?

Tri-aryl compounds can be synthesized through a variety of methods, including Friedel-Crafts acylation, Suzuki-Miyaura cross-coupling, and Sonogashira coupling. These reactions involve combining aromatic compounds with other reagents under specific reaction conditions to form the desired tri-aryl compound.

What are the properties of tri-aryl compounds?

Tri-aryl compounds have a wide range of properties, depending on the specific structure and functional groups present. In general, they are highly stable and have high melting and boiling points. They also exhibit strong UV absorption and fluorescence, making them useful in applications such as dyes and pigments.

What are some applications of tri-aryl compounds?

Tri-aryl compounds have a wide range of applications in various industries. They are commonly used in the production of pharmaceuticals, agrochemicals, and materials such as polymers and liquid crystals. They can also be used as dyes, pigments, and fluorescent probes in biological imaging.

What are the potential hazards of working with tri-aryl compounds?

As with any chemical, it is important to handle tri-aryl compounds with caution. Some potential hazards include skin and eye irritation, respiratory irritation, and potential carcinogenic effects. It is important to follow proper safety protocols and handle these compounds in a well-ventilated area.

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