• 1. Ester-mediated peptide formation promoted by deep eutectic solvents: a facile pathway to proto-peptides?
  Chen-Yu Chien,Sheng-Sheng Yu Chem. Commun., 2020,56, 11949-11952
• 2. Fate of nitrogen-15 in the subsequent growing season of greenhouse tomato plants (Lycopersicon esculentum Mill) as influenced by alternate partial root-zone irrigation
  Maomao Hou,Fenglin Zhong,Qiu Jin,Enjiang Liu,Jie Feng,Tengyun Wang,Yue Gao RSC Adv., 2017,7, 34392-34400
• 3. Excimer emission and magnetoluminescence of radical-based zinc(ii) complexes doped in host crystals?
  Shojiro Kimura,Tetsuro Kusamoto Chem. Commun., 2020,56, 11195-11198
• 4. 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
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Chlorobenzenes
• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Halobenzenes Chlorobenzenes

Comprehensive Overview of 3-(2,4-Dichlorophenyl)-1-propene (CAS No. 135439-18-8)

3-(2,4-Dichlorophenyl)-1-propene, with the CAS number 135439-18-8, is an organic compound that has garnered significant attention in the fields of chemical synthesis and material science. This compound, characterized by its dichlorophenyl and propene functional groups, serves as a versatile intermediate in the production of various specialty chemicals. Its unique structure makes it valuable for applications ranging from pharmaceuticals to agrochemicals, aligning with current trends in sustainable and efficient chemical processes.

The growing interest in 3-(2,4-Dichlorophenyl)-1-propene is partly driven by its role in the development of advanced materials and bioactive molecules. Researchers and industry professionals frequently search for terms like "synthesis of 3-(2,4-Dichlorophenyl)-1-propene" or "applications of CAS 135439-18-8," reflecting the demand for detailed technical insights. This compound's stability and reactivity under controlled conditions make it a subject of ongoing studies, particularly in green chemistry initiatives aimed at reducing environmental impact.

One of the key advantages of 3-(2,4-Dichlorophenyl)-1-propene lies in its adaptability to modular synthesis approaches. Modern chemical industries prioritize scalability and cost-effectiveness, and this compound fits well into such frameworks. Searches for "buy 3-(2,4-Dichlorophenyl)-1-propene" or "suppliers of CAS 135439-18-8" highlight its commercial relevance. Additionally, its potential use in polymer chemistry and catalysis aligns with the broader shift toward high-performance materials.

From a safety and handling perspective, 3-(2,4-Dichlorophenyl)-1-propene requires standard laboratory precautions, as with many organic intermediates. Discussions around "storage conditions for 135439-18-8" or "handling guidelines for dichlorophenyl compounds" are common among professionals. Proper documentation and compliance with regulatory standards ensure its safe utilization in research and industrial settings.

In summary, 3-(2,4-Dichlorophenyl)-1-propene (CAS No. 135439-18-8) represents a critical building block in modern chemistry. Its multifaceted applications, combined with the industry's focus on innovation and sustainability, underscore its importance. As research continues to uncover new uses, this compound is poised to remain a topic of interest for scientists and engineers alike.

• 1587-07-1(3-(2-Chlorophenyl)-1-propene)
• 842124-22-5(3-(4-Chloro-3-methylphenyl)-1-propene)
• 3047-25-4(4-(2-Chlorophenyl)-1-butene)
• 117269-67-7(4-(2,6-Dichlorophenyl)-1-butene)
• 62120-70-1(Benzene, 1,1'-(1,2-ethanediyl)bis[2,6-dichloro-)
• 33407-02-2(1,3-dichloro-2-ethylbenzene)
• 93794-95-7(3-(2,5-Dichlorophenyl)-1-propene)
• 90794-46-0(3-(2-Chlorophenyl)-2-methyl-1-propene)
• 3047-22-1(4-(2,4-Dichlorophenyl)-1-butene)
• 308360-40-9(Benzene, 1-chloro-2-(1-methyl-2-propenyl)-)