What is the chemical structure of %60%2528E%2529-6-%255B%2528E%2529-3-%25281-Pyrrolidinyl%2529-1-p-tolylpropenyl%255D-2-pyridineacrylic%2BAcid%60?

To determine the chemical structure of (E)-6-[(E)-3-(1 - Pyrrolidinyl)-1-p-tolylpropenyl]-2 - pyridineacrylic Acid, we break down the name step by step.
First, consider the main part related to the pyridine ring.Consider first the main part relating to the pyridine chain. The compound has a pyridine ring, which is a six - membered aromatic heterocycle with one nitrogen atom.The compound contains a pyridine heterocycle, which is a six-membered aromatic heterocycle containing one nitrogen atom. At the 2 - position of the pyridine ring, there is an acrylic acid group attached.The acrylic acid group is attached to the 2 - position on the pyridine. An acrylic acid group has the structure CH=CH - COOH, where the double bond has a particular geometry denoted by the overall (E) configuration for the whole molecule, indicating that the high - priority groups on either side of the double bond are on opposite sides.The structure of an acrylic acid group is CH=CH-COOH. The double bond has a specific geometry, which is indicated by the overall (E), configuration for the entire molecule. This indicates that the high-priority groups on either side are on the opposite sides.

Next, at the 6 - position of the pyridine ring, there is a more complex substituent.At the 6 -position of the pyridine, a more complex substitute is present. This substituent contains another double - bonded structure.This substituent has another double-bonded structure. Starting with the part (E)-3-(1 - Pyrrolidinyl)-1 - p - tolylpropenyl.Start with the part (E).3-(1- Pyrrolidinyl),-1-p-tolylpropenyl. The pyrrolidinyl group is a five - membered heterocyclic ring with one nitrogen atom.The pyrrolidinyl ring is a five-membered heterocyclic with one nitrogen atom. It is attached to the third carbon of a propenyl chain.It is attached to a third carbon in a propenyl ring.

The p - tolyl group is a benzene ring with a methyl group attached at the para position relative to the point of attachment to the rest of the molecule.The p-tolyl group is composed of a benzene group with a methyl attached at the para position in relation to the point of attachment of the rest of molecule. This p - tolyl group is attached to the first carbon of the propenyl chain.This p-tolyl group is attached at the first carbon in the propenyl ring. The double bond in this part of the substituent also has an (E) configuration, meaning that the high - priority groups around this double bond are on opposite sides.The double bond in the substituent has also an (E) configuration. This means that the high-priority groups around this double bonded are on the opposite side.

Combining all these parts, we can construct the overall chemical structure.We can build the overall chemical structure by combining all these parts. The pyridine ring forms the core, with the 2 - position having the acrylic acid side - chain and the 6 - position having the long, complex side - chain containing the pyrrolidinyl, p - tolyl, and propenyl components.The pyridine ring is the core. The 2 - position has the acrylic acid side-chain and the 6 – position has the long, complex, side-chain containing the pyrrolidinyl and p – tolyl components. Each part is connected through carbon - carbon bonds, with the double bonds having the (E) geometric configuration as specified in the name.Each part is linked by carbon-carbon bonds. The double bonds have the geometric configuration (E) as specified in its name. Overall, the molecule has a relatively complex structure with multiple aromatic and heterocyclic components, as well as unsaturated carbon - carbon double bonds and a carboxylic acid functional group which can participate in various chemical reactions due to their reactivity.The molecule is a complex one with many aromatic and heterocyclic compounds, as well as unsaturated double carbon-carbon bonds and a functional carboxylic group that can participate in a variety of chemical reactions because of their reactivity.

What are the applications of %60%2528E%2529-6-%255B%2528E%2529-3-%25281-Pyrrolidinyl%2529-1-p-tolylpropenyl%255D-2-pyridineacrylic%2BAcid%60?

"(E)-6-[(E)-3-(1-Pyrrolidinyl)-1-p-tolylpropenyl]-2-pyridineacrylic Acid" likely has applications in several areas.
In the field of medicinal chemistry, it may serve as a potential lead compound for drug development.It may be used as a lead compound in the field of medicinal chemical. Compounds with similar structures often show biological activities such as interacting with specific receptors or enzymes in the body.Compounds that have similar structures are often biologically active, interacting with specific enzymes or receptors in the body. For example, the pyridine and acrylic acid moieties can potentially participate in hydrogen bonding and other non - covalent interactions with biological targets.The pyridine and the acrylic acid moiety can participate in hydrogen bonds and other non-covalent interactions with biological targets. The pyrrolidinyl and p - tolyl groups may influence the lipophilicity and binding affinity of the molecule.The pyrrolidinyl or p-tolyl groups can influence the binding affinity and lipophilicity of the molecule. If it can bind to a disease - related receptor, it could be developed into a drug for treating conditions like certain types of cancers where abnormal receptor signaling is involved, or neurodegenerative diseases where specific enzyme regulation is crucial.If it can bind a disease-related receptor, it could become a drug to treat conditions like certain types cancers, where abnormal receptor signaling may be involved, or neurodegenerative disorders, where specific enzyme regulation plays a crucial role.

In materials science, it might be used in the synthesis of functional polymers.In materials science, this polymer could be used to synthesize functional polymers. The double bonds in the acrylic acid part can be polymerized, and the rest of the complex structure can introduce unique properties to the resulting polymer.The double bonds of the acrylic acid can be polymerized and the rest can give the polymer unique properties. For instance, the pyridine group can potentially coordinate with metal ions, enabling the creation of polymers with metal - binding capabilities.The pyridine group, for example, can potentially coordinate with metallic ions to enable the creation of polymers that have metal-binding capabilities. These polymers could be used in applications such as selective metal ion extraction from industrial wastewaters or in the development of sensors.These polymers can be used for applications such as the selective extraction of metal ions from industrial wastewaters, or in the development and manufacture of sensors. The specific combination of groups in this compound can also affect the solubility and mechanical properties of the polymer, making it suitable for different material - based applications like coatings or membranes.The combination of groups within this compound can affect the solubility of the polymer and its mechanical properties, making it suitable for a variety of material-based applications such as coatings or membranes.

In chemical research, it can act as a building block for the synthesis of more complex molecules.In chemical research, it is used as a building-block for the synthesis more complex molecules. Chemists can use its reactive functional groups to perform various organic reactions.Chemists use its reactive functional group to perform different organic reactions. The double bonds can be subject to addition reactions, while the carboxylic acid group can be used in esterification or amide - formation reactions.The double bonds are subject to addition reactions while the carboxylic acids can be used for esterification and amide-formation reactions. By modifying this compound further, researchers can create libraries of related compounds for structure - activity relationship studies.Researchers can create libraries of compounds related to this compound for structure-activity relationship studies by further modifying it. These studies help in understanding how changes in the molecular structure affect properties such as biological activity, physical characteristics, or reactivity, which is essential for the advancement of organic chemistry as a whole.These studies are essential to the advancement of organic chemical chemistry because they help understand how changes in molecular structures affect properties like biological activity, physical properties, or reactivity.

What are the properties of %60%2528E%2529-6-%255B%2528E%2529-3-%25281-Pyrrolidinyl%2529-1-p-tolylpropenyl%255D-2-pyridineacrylic%2BAcid%60?

( E ) -6 - [( E ) -3 - (1 - Pyrrolidinyl) -1 - p - tolylpropenyl] -2 - pyridineacrylic Acid likely has several properties.The properties of ( E ), -6 – [( E) -3 – (1 - Pyrrolidinyl), -1 - P - Tolylpropenyl]-2 - pyridineacrylic Acid are likely to be several.
First, in terms of its physical properties, it is likely a solid at room temperature given its relatively complex molecular structure with multiple aromatic and heterocyclic rings.In terms of its physical properties at room temperature, it is probably a solid due to its relatively complex molecular structures with multiple aromatic and homocyclic rings. Solubility is an important aspect.Solubility is a key factor. The presence of polar groups such as the carboxylic acid group (-COOH) and the pyridine ring would suggest some solubility in polar solvents like water, ethanol, and methanol.The presence of polar groupings such as the carboxylic acids (-COOH) or the pyridine rings would suggest that the compound is soluble in polar solvents, like water, alcohol, and methanol. However, the non - polar components, including the tolyl group and the pyrrolidinyl group, would limit its solubility in water and increase its solubility in less polar organic solvents such as dichloromethane or ethyl acetate.The non-polar components such as the tolyl and pyrrolidinyl groups would limit its solubility and increase its solubility when it is in less polar organic solutions like dichloromethane and ethyl anacetate.

Chemically, the carboxylic acid group is highly reactive.Chemically, carboxylic acid is highly reactive. It can participate in acid - base reactions, donating a proton to form a carboxylate anion in the presence of a base.It can participate in acid-base reactions, donating an electron to form a carboxylate ion in the presence a base. This property can be used in the synthesis of salts, which may have different solubility and stability profiles compared to the free acid.This property can also be used to synthesize salts that have different solubility profiles and stability profiles than the free acid. The double bonds in the molecule, both in the propenyl moieties, are sites of electrophilic addition reactions.The double bonds of the molecule are the sites for electrophilic additions. They can react with reagents such as halogens, hydrogen halides, or water in the presence of appropriate catalysts.In the presence of catalysts, they can react with reagents like halogens or hydrogen halides. The pyridine ring also has its own reactivity.The pyridine rings also have their own reactivity. It can act as a weak base due to the lone pair of electrons on the nitrogen atom, and can participate in reactions with electrophiles.It can act as an electrophile and a weak base because of the lone electron pair on the nitrogen atom.

In terms of its potential biological properties, the presence of the pyridine and aromatic rings may allow it to interact with biological targets through hydrophobic interactions.The presence of the aromatic and pyridine rings could allow it to interact with targets via hydrophobic interactions. The carboxylic acid group could potentially bind to proteins or enzymes through hydrogen bonding or ionic interactions if the target has complementary binding sites.The carboxylic group may bind to enzymes or proteins through hydrogen bonding, ionic interactions or complementary binding sites. It may have applications in drug discovery, as molecules with similar structural features often show activities such as antibacterial, antifungal, or anti - inflammatory properties.It could be used in drug discovery as molecules with similar structures often have antibacterial, antifungal or anti-inflammatory properties. However, further in - vitro and in - vivo studies would be required to fully explore its biological potential.Further in - vitro or in vivo studies are needed to fully explore the biological potential of this compound.

Overall, the combination of polar and non - polar regions, along with multiple reactive functional groups, gives ( E ) -6 - [( E ) -3 - (1 - Pyrrolidinyl) -1 - p - tolylpropenyl] -2 - pyridineacrylic Acid a rich set of physical and chemical properties that can be exploited in various fields such as organic synthesis, materials science, and potentially in the development of bioactive compounds.The combination of polar and a non-polar region, along with multiple functional groups, gives the ( E ), -6 – [( E ), -3 – (1 - Pyrrolidinyl), -1 -p -tolylpropenyl]-2 -pyridineacrylic Acid an array of physical and chemical characteristics that can be exploited by various fields, such as organic synthesis and materials science.

What is the synthesis method of %60%2528E%2529-6-%255B%2528E%2529-3-%25281-Pyrrolidinyl%2529-1-p-tolylpropenyl%255D-2-pyridineacrylic%2BAcid%60?

The synthesis of (E)-6-[(E)-3-(1 - Pyrrolidinyl)-1 - p - tolylpropenyl]-2 - pyridineacrylic acid typically involves several steps.The synthesis of (E-6)-6-[(E-3)-(1-Pyrrolidinyl),-1-p-tolylpropenyl]-2-pyridineacrylic acids typically involves multiple steps.
First, start with the appropriate pyridine and toluene derivatives.Start with the appropriate pyridine derivatives and toluene. For example, 2 - pyridineacrylic acid derivatives can be prepared through Knoevenagel condensation.Knoevenagel condensation can be used to prepare derivatives of 2 -pyridineacrylic acids. React a 2 - formylpyridine with malonic acid in the presence of a base such as piperidine and a suitable solvent like pyridine.React malonic acid with a 2 – formylpyridine in the presence a base like piperidine, and a suitable solvant like pyridine. This reaction forms the 2 - pyridineacrylic acid moiety with the characteristic double bond in the (E) - configuration due to the thermodynamic control of the reaction conditions.The thermodynamic control of reaction conditions allows the formation of the 2 -pyridineacrylic moiety with its characteristic double bond in (E)- configuration.

Next, the (E)-3-(1 - Pyrrolidinyl)-1 - p - tolylpropenyl part needs to be synthesized.The next step is to synthesize the (E-3)-3-(1- Pyrrolidinyl-1)-1-p-tolylpropenyl. React p - toluyl chloride with pyrrolidine to form an intermediate.React p-toluylchloride with pyrrolidine in order to form an intermediary. Then, through Wittig - type reactions or Horner - Wadsworth - Emmons reactions, introduce a double bond.Then, using Wittig-type reactions or Horner-Wadsworth-Emmons reactions, introduce the double bond. For instance, react the intermediate with a phosphorus ylide or a phosphonate ester to create the (E)-3-(1 - Pyrrolidinyl)-1 - p - tolylpropenyl fragment.React the intermediate with either a phosphorus ester or a phosphorus-ylide to produce the (E)-3 - (1 - Pyrrolidinyl )-1 -p -tolylpropenyl fraction.

Finally, couple the two key fragments together.Couple the two fragments. This can be achieved through a cross - coupling reaction such as a Heck reaction.This can be done by a Heck reaction or a cross-coupling reaction. React the 2 - pyridineacrylic acid derivative with the (E)-3-(1 - Pyrrolidinyl)-1 - p - tolylpropenyl fragment in the presence of a palladium catalyst, a base, and a suitable ligand.In the presence of a palladium catalyst, a base and a suitable ligand, react the 2 pyridineacrylic acids derivative with the (E )-3-(1-pyrrolidinyl )-1 p – tolylpropenyl fraction. The reaction conditions, including the choice of solvent (such as DMF or toluene), temperature, and reaction time, need to be carefully optimized to ensure high yield and good selectivity for the desired product.To ensure high yields and selectivity, the reaction conditions must be optimized. This includes the choice of solvent, such as DMF or TOLUENE, temperature, and time. After the reaction is complete, the product can be isolated and purified through techniques like column chromatography and recrystallization to obtain pure (E)-6-[(E)-3-(1 - Pyrrolidinyl)-1 - p - tolylpropenyl]-2 - pyridineacrylic acid.After the reaction, the product can then be isolated and purified using techniques such as column chromatography or recrystallization.

What are the safety hazards of %60%2528E%2529-6-%255B%2528E%2529-3-%25281-Pyrrolidinyl%2529-1-p-tolylpropenyl%255D-2-pyridineacrylic%2BAcid%60?

( E ) -6 - [( E ) -3 - (1 - Pyrrolidinyl) -1 - p - tolylpropenyl] -2 - pyridineacrylic Acid is a chemical compound.Chemical compound (E )-6 - [(E )-3 -1 pyrrolidinyl] -1 p-tolylpropenyl]-2 pyridineacrylic Acid. Identifying its safety hazards often requires in - depth chemical and toxicological knowledge and research on the specific properties of this molecule.To identify its safety hazards, it is often necessary to have a thorough understanding of the chemistry and toxicology and research into the specific properties.
Regarding potential physical hazards, if it is in powder form, there could be a risk of dust explosion under certain conditions.Under certain conditions, powders could cause a dust explosion. Finely divided powders can form explosive mixtures with air when dispersed in appropriate concentrations and ignited by a source of ignition.When finely divided powders are dispersed and ignited with air, they can form explosive mixtures.

In terms of health hazards, skin contact might lead to irritation.Skin contact could cause irritation. The compound could potentially disrupt the normal function of the skin's barrier, causing redness, itching, or in more severe cases, dermatitis.The compound may disrupt the normal function and structure of the skin barrier, leading to redness, itching or, in more severe cases dermatitis. This is because many organic compounds can interact with the skin's proteins and lipids, altering their normal structure and function.Many organic compounds can alter the normal structure and function of skin lipids and proteins.

Eye contact is likely to be a significant hazard.Contact with the eyes is likely to pose a serious risk. The compound may cause severe eye irritation, potentially damaging the cornea and other eye tissues.The compound can cause severe eye irritation and damage the cornea or other eye tissues. It could lead to pain, watering, and blurred vision.It can cause pain, tearing, and blurred sight. Immediate and thorough rinsing of the eyes is crucial in case of exposure.In the event of exposure, it is important to rinse your eyes immediately and thoroughly.

Inhalation of its dust or vapor (if it has a significant vapor pressure) can pose risks to the respiratory system.Inhaling its dust or vapor can be harmful to the respiratory system (if it has significant vapor pressure). It might irritate the nasal passages, throat, and lungs.It can irritate nasal passages, the throat, and the lungs. Prolonged or high - level inhalation could potentially lead to more serious respiratory problems such as coughing, shortness of breath, and in extreme cases, damage to the lung parenchyma.Inhalation at high levels or for long periods of time can cause respiratory problems, such as coughing and shortness-of-breath, and, in extreme cases, lung damage.

There may also be concerns about its potential toxicity if ingested.Its potential toxicity, if consumed, may also raise concerns. It could cause harm to the digestive system, leading to symptoms like nausea, vomiting, abdominal pain, and potentially more serious internal organ damage depending on the amount ingested and the compound's specific toxicological profile.It can cause digestive problems, resulting in symptoms such as nausea, vomiting and abdominal pain. More serious internal organ damage could also occur depending on the amount consumed and the compound's toxicological profile.

Furthermore, like many synthetic organic compounds, there may be long - term health risks such as mutagenicity (the potential to cause changes in DNA), carcinogenicity (the potential to cause cancer), or reproductive toxicity.Like many synthetic organic compounds, this chemical may also pose long-term health risks, such as mutagenicity, carcinogenicity, or reproductive toxicity. However, definite conclusions about these long - term risks would require specific toxicological studies on this particular chemical.To be able to draw definitive conclusions about the long-term risks, specific toxicological studies would need to be conducted on this chemical.