3-(4-nitrophenyl)acrylic Acid


Properties

product_name 3-(4-Nitrophenyl)acrylic acid
CAS_number 555-17-3
formula C9H7NO4
molar_mass 193.16 g/mol
property_1 Yellow crystalline solid
property_2 Melting Point: 209-212°C
property_3 Boiling Point: Not applicable (decomposes)
property_4 Solubility: Sparingly soluble in water
property_5 Density: Not readily available
property_6 PKa: Not readily available
property_7 LogP: Not readily available
property_8 Refractive Index: Not readily available
property_9 Vapor Pressure: Not readily available
property_10 Hazard Classification: May be an irritant or harmful if swallowed or inhaled

FAQ

What is 3-(4-Nitrophenyl)acrylic acid?

3-(4-Nitrophenyl)acrylic acid is a compound that belongs to the class of acrylic acids. It is commonly used in organic synthesis and chemical research due to its unique properties and applications.

What are the main uses of 3-(4-Nitrophenyl)acrylic acid?

3-(4-Nitrophenyl)acrylic acid is primarily used as a key intermediate in the synthesis of various organic compounds, such as pharmaceuticals, agrochemicals, and dyes. It is also employed as a building block in the development of new materials and fine chemicals.

What are the key properties of 3-(4-Nitrophenyl)acrylic acid?

3-(4-Nitrophenyl)acrylic acid is a crystalline solid that is light yellow in color. It is soluble in common organic solvents such as ethanol, acetone, and dichloromethane. The compound has a molecular weight of around 235.2 g/mol and a melting point of approximately 130-132°C.

How is 3-(4-Nitrophenyl)acrylic acid synthesized?

3-(4-Nitrophenyl)acrylic acid can be synthesized through a multi-step reaction starting from commercially available starting materials. The typical route involves the condensation of 4-nitrobenzaldehyde with malonic acid followed by decarboxylation and acid hydrolysis to yield the final product.

What are the benefits of using 3-(4-Nitrophenyl)acrylic acid in organic synthesis?

One of the main advantages of using 3-(4-Nitrophenyl)acrylic acid is its versatility as a building block for various chemical transformations. It can be easily modified to introduce different functional groups and enhance the reactivity of the final compound. Additionally, the presence of the nitro group offers unique opportunities for further derivatization.

Are there any safety considerations when handling 3-(4-Nitrophenyl)acrylic acid?

As with any chemical compound, it is important to handle 3-(4-Nitrophenyl)acrylic acid with care and follow proper safety protocols. The compound should be used in a well-ventilated area, and personal protective equipment such as gloves and goggles should be worn to prevent contact with the skin or eyes. In case of ingestion or skin exposure, medical attention should be sought immediately.

Can 3-(4-Nitrophenyl)acrylic acid be customized for specific research needs?

Yes, 3-(4-Nitrophenyl)acrylic acid can be customized and synthesized according to specific research requirements. By modifying the reaction conditions or introducing additional functional groups, the properties of the compound can be tailored to meet the desired objectives of the study.

What are the storage recommendations for 3-(4-Nitrophenyl)acrylic acid?

3-(4-Nitrophenyl)acrylic acid should be stored in a cool, dry place away from direct sunlight and sources of heat. The compound should be kept in a tightly sealed container to prevent moisture absorption and degradation. Proper labeling and tracking of the storage conditions are essential to maintain the quality and stability of the product.

In what ways can 3-(4-Nitrophenyl)acrylic acid contribute to the advancement of chemical research?

3-(4-Nitrophenyl)acrylic acid offers a valuable platform for exploring new synthetic methodologies and developing innovative chemical processes. Its unique structure and reactivity make it a valuable tool for investigating reaction mechanisms, designing novel molecules, and advancing the frontiers of organic chemistry. By incorporating 3-(4-Nitrophenyl)acrylic acid into research projects, scientists can broaden their understanding of chemical transformations and potentially discover new applications for this versatile compound.