• 1. An asymmetric supercapacitor based on controllable WO3 nanorod bundle and alfalfa-derived porous carbon?
  Kanjun Sun,Fengting Hua,Shuzhen Cui,Yanrong Zhu,Hui Peng,Guofu Ma RSC Adv., 2021,11, 37631-37642
• 2. An atlas of endohedral Sc2S cluster fullerenes?
  Li-Hua Gan,Rui Wu,Jian-Lei Tian,Patrick W. Fowler Phys. Chem. Chem. Phys., 2017,19, 419-425
• 3. An aptasensor for detection of potassium ions based on RecJf exonuclease mediated signal amplification
  Bidou Wang,Xifeng Chen Analyst, 2014,139, 5695-5699
• 4. An amorphous Cu–In–S nanoparticle-based precursor ink with improved atom economy for CuInSe2 solar cells with 10.85% efficiency?
  Green Chem., 2017,19, 1268-1277
• 5. Aggregation kinetics and gel formation in modestly concentrated suspensions of oppositely charged model ceramic colloids: a numerical study
  M. A. Piechowiak,A. Videcoq,R. Ferrando,D. Bochicchio,C. Pagnoux,F. Rossignol Phys. Chem. Chem. Phys., 2012,14, 1431-1439

• Solvents and Organic Chemicals Organic Compounds Hydrocarbons Unsaturated hydrocarbons Branched unsaturated hydrocarbons

Exploring the Versatile Applications of Bicyclo[2.2.1]hept-2-ene, 2-methyl- (CAS No. 694-92-8)

Bicyclo[2.2.1]hept-2-ene, 2-methyl- (CAS No. 694-92-8) is a fascinating bicyclic organic compound that has garnered significant attention in both academic and industrial research. This compound, often referred to as 2-methylnorbornene, belongs to the norbornene family and is characterized by its unique bicyclic structure. Its molecular formula is C₈H₁₂, and it features a double bond within the bicyclic framework, making it a valuable intermediate in organic synthesis and polymer chemistry.

The chemical properties of Bicyclo[2.2.1]hept-2-ene, 2-methyl- make it a versatile building block for various applications. Its strained ring system and reactive double bond allow it to participate in a wide range of chemical reactions, including ring-opening metathesis polymerization (ROMP) and Diels-Alder reactions. These reactions are pivotal in the development of advanced materials, such as high-performance polymers and specialty chemicals. Researchers are particularly interested in its potential for creating functionalized polymers with tailored properties.

One of the most exciting applications of Bicyclo[2.2.1]hept-2-ene, 2-methyl- is in the field of material science. Its ability to form cross-linked polymers with exceptional thermal and mechanical stability has made it a popular choice for developing coatings, adhesives, and composites. In recent years, the demand for sustainable materials has surged, and this compound has been explored as a key component in bio-based polymers. Its compatibility with green chemistry principles aligns well with the global push toward environmentally friendly solutions.

Another area where Bicyclo[2.2.1]hept-2-ene, 2-methyl- shines is in pharmaceutical research. The compound's rigid structure serves as a scaffold for designing novel drug candidates. Medicinal chemists leverage its stereochemical properties to create molecules with enhanced bioavailability and target specificity. Recent studies have investigated its derivatives for potential anti-inflammatory and antiviral activities, reflecting the growing interest in drug discovery and personalized medicine.

The industrial significance of Bicyclo[2.2.1]hept-2-ene, 2-methyl- cannot be overstated. It is widely used in the production of elastomers and rubber modifiers, where its incorporation improves material performance under extreme conditions. Additionally, its role in catalysis and organic synthesis has been extensively documented, with applications ranging from fine chemicals to agrochemicals. The compound's adaptability to various reaction conditions makes it a favorite among chemists working on process optimization and scale-up.

From a market perspective, the demand for Bicyclo[2.2.1]hept-2-ene, 2-methyl- is expected to grow steadily, driven by advancements in polymer technology and green chemistry. Companies specializing in specialty chemicals are investing in research to expand its applications, particularly in renewable energy and electronics. For instance, its derivatives are being tested as components in organic semiconductors, which are crucial for next-generation flexible electronics and solar cells.

For researchers and industry professionals seeking reliable information on Bicyclo[2.2.1]hept-2-ene, 2-methyl-, it is essential to consider its safety data and handling protocols. While the compound is not classified as hazardous under standard regulations, proper laboratory practices should always be followed. Its storage conditions, solubility, and reactivity profiles are well-documented, ensuring safe usage in both academic and industrial settings.

In conclusion, Bicyclo[2.2.1]hept-2-ene, 2-methyl- (CAS No. 694-92-8) is a multifaceted compound with immense potential across diverse fields. Its unique chemical structure, coupled with its broad applicability, positions it as a cornerstone in modern chemistry. Whether in advanced materials, pharmaceuticals, or industrial processes, this compound continues to inspire innovation and drive progress. As research evolves, its role in addressing global challenges, such as sustainability and healthcare, will undoubtedly expand.

• 61888-36-6(Bicyclo[2.2.1]hept-2-en-7-ylidene, 2-methyl-)
• 529-16-8(Bicyclo[2.2.1]hept-2-ene,2,3-dimethyl-)
• 67003-10-5(4,7-Methano-1H-indene, 3a,4,7,7a-tetrahydro-3,5-dimethyl-)
• 87386-00-3(4,7-Methano-1H-indene, 3a,4,7,7a-tetrahydro-3,6-dimethyl-)
• 88418-19-3(Bicyclo[2.2.1]hept-2-en-7-yl, 2,3-dimethyl-)
• 89521-29-9(Bicyclo[2.2.1]hept-2-ene,2-methyl-6-(1-methylethyl)-, exo- (9CI))
• 86954-77-0(NISTC86954770)
• 26472-00-4(Methylcyclopentadiene dimer)
• 7570-08-3(4,7-Methano-1H-indene, 3a,4,7,7a-tetrahydro-2,5-dimethyl-)
• 15819-46-2(2-Butenyl)