3-Cyclohexene-1-carboxaldehyde is a chemical compound that plays a significant role in everyday life. It is commonly used in the production of perfumes, flavorings, and pharmaceuticals. Its aromatic properties make it a valuable ingredient in various consumer products, enhancing their scent and taste. Additionally, 3-Cyclohexene-1-carboxaldehyde is utilized in research and development for its versatile applications in organic synthesis. Overall, this compound contributes to the creation of products that enhance the sensory experience in our daily lives.
Table of Contents:
- 💡 Commercial Applications
- ⚗️ Chemical & Physical Properties
- 🏭 Production & Procurement
- ⚠️ Safety Considerations
- 🔬 Potential Research Directions
- 🧪 Related Compounds
💡 Commercial Applications
3-Cyclohexene-1-carboxaldehyde, also known as 3-Cyclohexene-1-formaldehyde, has various commercial and industrial applications. This compound is commonly used as a precursor in the synthesis of pharmaceuticals, fragrances, and other organic compounds. Its unique chemical structure makes it a versatile building block for creating more complex molecules.
In the pharmaceutical industry, 3-Cyclohexene-1-carboxaldehyde is utilized in the synthesis of various drugs and medications. Its reactivity and compatibility with other compounds make it a valuable intermediate in the production of pharmaceutical products. This compound plays a crucial role in the development of novel drug formulations and treatments for various medical conditions.
3-Cyclohexene-1-carboxaldehyde also finds applications in the fragrance and flavor industry. It is used as a key ingredient in the creation of perfumes, essential oils, and food additives. The compound’s aromatic properties contribute to the pleasant scents and flavors of these products, making it a sought-after component in the production of fragrances and flavoring agents.
⚗️ Chemical & Physical Properties
3-Cyclohexene-1-carboxaldehyde is a colorless liquid with a pungent, unpleasant odor. This compound is most commonly used in the production of fragrances, flavors, and pharmaceuticals due to its distinctive scent.
With a molar mass of 120.15 g/mol and a density of 0.941 g/cm³, 3-Cyclohexene-1-carboxaldehyde is relatively light compared to common food items like sugar (molar mass of 342.3 g/mol) and olive oil (density of 0.92 g/cm³).
The melting point of 3-Cyclohexene-1-carboxaldehyde is -48.5°C, while the boiling point is 167°C. These values are significantly lower than those of common food items like butter (melting point of 32°C) and water (boiling point of 100°C).
3-Cyclohexene-1-carboxaldehyde is sparingly soluble in water and has a low viscosity. This contrasts with common food items like salt (high solubility in water) and honey (high viscosity), highlighting the differences in their chemical and physical properties.
🏭 Production & Procurement
3-Cyclohexene-1-carboxaldehyde, a cyclic compound with a carboxaldehyde functional group, is commonly produced through the oxidation of cyclohexene. This process typically involves reacting cyclohexene with a strong oxidizing agent, such as potassium permanganate or chromic acid, under controlled conditions. The resulting intermediate is then further oxidized to yield 3-Cyclohexene-1-carboxaldehyde.
Procuring 3-Cyclohexene-1-carboxaldehyde commercially involves contacting chemical suppliers or manufacturers who specialize in producing and distributing this compound. It is commonly available in liquid form or as a solid, and it is essential to ensure that proper safety precautions and regulations are followed when handling and transporting the substance. 3-Cyclohexene-1-carboxaldehyde can be transported in containers that are compatible with its properties to prevent leakage or contamination during transit.
Transporting 3-Cyclohexene-1-carboxaldehyde requires adherence to regulations regarding the transportation of hazardous chemicals. It is crucial to ensure that the compound is securely packaged and labeled according to relevant guidelines to prevent accidents or mishandling during transit. Additionally, it is recommended to work with reputable transportation companies that have experience in handling and transporting hazardous chemicals to ensure the safe delivery of 3-Cyclohexene-1-carboxaldehyde to its intended destination.
⚠️ Safety Considerations
Safety considerations for 3-Cyclohexene-1-carboxaldehyde include its potential to cause skin irritation, eye irritation, and respiratory irritation. It is important to handle this chemical with proper protective equipment, such as gloves, goggles, and a lab coat. In case of contact with skin or eyes, it is important to rinse thoroughly with water and seek medical attention if necessary. Additionally, 3-Cyclohexene-1-carboxaldehyde should be stored in a cool, dry, well-ventilated area away from incompatible materials to prevent accidents or interactions that could lead to hazardous situations.
The hazard statements for 3-Cyclohexene-1-carboxaldehyde include “Causes skin irritation,” “Causes serious eye irritation,” and “May cause respiratory irritation.” These statements indicate the potential risks associated with exposure to this chemical, highlighting the importance of handling it with care and following proper safety protocols to minimize the likelihood of harm. It is important to be aware of these hazards when working with 3-Cyclohexene-1-carboxaldehyde to ensure the safety of laboratory personnel and prevent accidents or injuries.
Precautionary statements for 3-Cyclohexene-1-carboxaldehyde include “Wear protective gloves/eye protection/face protection” and “Avoid breathing dust/fume/gas/mist/vapors/spray.” These statements emphasize the importance of using personal protective equipment when handling this chemical to protect against skin and eye irritation, as well as respiratory irritation. It is essential to follow these precautionary statements to minimize the risk of exposure to 3-Cyclohexene-1-carboxaldehyde and ensure the safety of individuals working with this compound.
🔬 Potential Research Directions
One potential research direction for 3-Cyclohexene-1-carboxaldehyde is the investigation of its use as a building block in organic synthesis. This compound is a valuable starting material for the synthesis of various cyclic compounds and could be studied further for its potential applications in the pharmaceutical and agrochemical industries.
Another potential area of research for 3-Cyclohexene-1-carboxaldehyde is its reactivity towards different reagents and conditions. Understanding the reactivity of this compound can lead to the development of new reactions and methodologies for the synthesis of complex molecules. This could open up new avenues for the discovery of novel drugs and materials.
Additionally, the study of the physical and chemical properties of 3-Cyclohexene-1-carboxaldehyde could provide valuable insights into its behavior in different environments. Researchers could explore its solubility, stability, and spectroscopic characteristics to gain a better understanding of its potential applications. This research could contribute to the development of more efficient synthetic routes and processes involving this compound.
🧪 Related Compounds
One similar compound to 3-Cyclohexene-1-carboxaldehyde is 2-Cyclohexene-1-carboxaldehyde. This compound also contains a cyclohexene ring and a carboxaldehyde functional group. However, the placement of the double bond on the second carbon atom in this compound distinguishes it from 3-Cyclohexene-1-carboxaldehyde.
Another analogous compound is Cyclohexene-1-carboxaldehyde. In this compound, the cyclohexene ring is present without any additional substituents. The carboxaldehyde functional group is attached to the carbon atom adjacent to the ring, giving the structure a distinct chemical nature compared to 3-Cyclohexene-1-carboxaldehyde.
Additionally, 3-Cyclohexene-1-carboxaldehyde is structurally similar to Cyclohexene-1-carboxylic acid. The major difference lies in the functional group attached to the cyclohexene ring. While 3-Cyclohexene-1-carboxaldehyde contains an aldehyde group, Cyclohexene-1-carboxylic acid possesses a carboxylic acid group. These compounds share a common cyclohexene ring structure but exhibit different chemical properties due to the variation in functional groups.
