• 1. Excitation dependent bidirectional electron transfer in phthalocyanine-functionalised MoS2 nanosheets?
  Christopher J. Harrison,Kyle J. Berean,Enrico Della Gaspera,Jian Zhen Ou,Richard B. Kaner,Kourosh Kalantar-zadeh,Torben Daeneke Nanoscale, 2016,8, 16276-16283
• 2. Dissociation of large gaseous serine clusters produces abundant protonated serine octamer
  Jacob S. Jordan,Evan R. Williams Analyst, 2021,146, 2617-2625
• 3. Estimates of hydride ion stability in condensed systems: energy of formation and solvation in aqueous and polar-organic solvents
  Craig A. Kelly,David R. Rosseinsky Phys. Chem. Chem. Phys., 2001,3, 2086-2090
• 4. Distinct correlation between (CN2)x units and pores: a low-cost method for predesigned wide range control of micropore size of porous carbon?
  Xiaotong Feng,Lei Bian,Jie Ma,Lei Zhou,Xiayan Wang,Guangsheng Guo,Qiaosheng Pu Chem. Commun., 2019,55, 3963-3966
• 5. Evolution of important glucosinolates in three common Brassica vegetables during their processing into vegetable powder and in vitro gastric digestion
  Nan Fu,Naphaporn Chiewchan,Xiao Dong Chen Food Funct., 2020,11, 211-220

Comprehensive Guide to 1H-Imidazole,2-ethyl-1-(2-propen-1-yl)- (CAS No. 14967-24-9): Properties, Applications, and Market Insights

1H-Imidazole,2-ethyl-1-(2-propen-1-yl)- (CAS No. 14967-24-9) is a specialized organic compound belonging to the imidazole family. This compound has garnered significant attention in recent years due to its unique chemical structure and versatile applications in pharmaceuticals, agrochemicals, and material science. Researchers and industry professionals frequently search for "1H-Imidazole derivatives" or "CAS 14967-24-9 applications" to understand its potential uses and benefits.

The molecular formula of 1H-Imidazole,2-ethyl-1-(2-propen-1-yl)- is C8H12N2, featuring an imidazole ring substituted with an ethyl group at the 2-position and an allyl group at the 1-position. This structural configuration contributes to its reactivity and functionality, making it a valuable intermediate in synthetic chemistry. Searches like "synthesis of 2-ethyl-1-(2-propen-1-yl)imidazole" highlight the growing interest in its preparation methods.

One of the most prominent applications of 1H-Imidazole,2-ethyl-1-(2-propen-1-yl)- is in the pharmaceutical industry, where it serves as a building block for drug development. Its imidazole core is a common motif in bioactive molecules, particularly in antifungal and antibacterial agents. Queries such as "imidazole-based pharmaceuticals" or "CAS 14967-24-9 in medicine" reflect the compound's relevance in modern therapeutics.

In agrochemicals, 1H-Imidazole,2-ethyl-1-(2-propen-1-yl)- is utilized in the synthesis of pesticides and herbicides. Its ability to interact with biological systems makes it an effective component in crop protection products. Industry professionals often search for "imidazole derivatives in agriculture" or "allyl-substituted imidazoles" to explore its agrochemical potential.

Material science is another field where 1H-Imidazole,2-ethyl-1-(2-propen-1-yl)- finds application. Its allyl group allows for polymerization and cross-linking, making it useful in the production of advanced polymers and coatings. Searches like "imidazole-based polymers" or "CAS 14967-24-9 in materials" indicate its growing importance in this sector.

The market for 1H-Imidazole,2-ethyl-1-(2-propen-1-yl)- is expanding, driven by increasing demand in pharmaceuticals and agrochemicals. Market analysts often track trends related to "imidazole compound demand" or "CAS 14967-24-9 suppliers" to gauge its commercial viability. The compound's versatility ensures its continued relevance in various industries.

From a regulatory perspective, 1H-Imidazole,2-ethyl-1-(2-propen-1-yl)- is subject to standard chemical safety guidelines. Researchers and manufacturers must adhere to protocols for handling and storage to ensure safety and compliance. Queries such as "safety data for CAS 14967-24-9" or "imidazole handling precautions" are common among professionals working with this compound.

In conclusion, 1H-Imidazole,2-ethyl-1-(2-propen-1-yl)- (CAS No. 14967-24-9) is a multifaceted compound with significant applications across multiple industries. Its unique chemical properties, coupled with its role in pharmaceuticals, agrochemicals, and material science, make it a subject of ongoing research and commercial interest. As the demand for specialized imidazole derivatives grows, this compound is poised to play an even more critical role in scientific and industrial advancements.

• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
• 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
• 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
• 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
• 89640-58-4(2-Iodo-4-nitrophenylhydrazine)
• 1449132-38-0(3-Fluoro-5-(2-fluoro-5-methylbenzylcarbamoyl)benzeneboronic acid)
• 2034271-14-0(2-(1H-indol-3-yl)-N-{[6-(thiophen-2-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl}acetamide)