• 1. Exciplex emission from the mixed dimer of naphthalene and 2-cyanonaphthalene in a supersonic jet
  Aloke Das,K. K. Mahato,Chayan K. Nandi,Tapas Chakraborty,Shridhar R. Gadre,Nikhil A. Gokhale Phys. Chem. Chem. Phys., 2002,4, 2162-2168
• 2. Excellent lithium ion storage property of porous MnCo2O4 nanorods?
  Peiyuan Zeng,Xiaoxiao Wang,Ming Ye,Qiuyang Ma,Jianwen Li,Wanwan Wang,Baoyou Geng,Zhen Fang RSC Adv., 2016,6, 23074-23084
• 3. Fe3O4 nanosphere@microporous organic networks: enhanced anode performances in lithium ion batteries through carbonization?
  Byungho Lim,Jaewon Jin,Jin Yoo,Seung Yong Han,Kyeongyeol Kim,Sungah Kang,Nojin Park,Sang Moon Lee,Hae Jin Kim,Seung Uk Son Chem. Commun., 2014,50, 7723-7726
• 4. Excellent electrochemical performance of LiFe0.4Mn0.6PO4 microspheres produced using a double carbon coating process?
  Yong Ping Huang,Tao Tao,Zheng Chen,Wei Han,Ying Wu,Chunjiang Kuang,Shaoxiong Zhou,Ying Chen J. Mater. Chem. A, 2014,2, 18831-18837
• 5. Excellent energy storage performance in NaNbO3-based relaxor antiferroeic ceramics under a low electric field
  XuxinCheng,XiaomingChen,PengyuanFan

• Solvents and Organic Chemicals Organic Compounds Organohalogen compounds Vinyl halides Vinyl bromides

3-Bromoprop-2-en-1-ol (CAS No. 37675-33-5)

3-Bromoprop-2-en-1-ol, also known as allyl bromide alcohol or 2-propenol with a bromine substituent, is a versatile organic compound with the CAS registry number 37675-33-5. This compound is characterized by its unique structure, which includes a bromine atom attached to the third carbon of a propenol chain. The molecule's structure allows it to participate in a wide range of chemical reactions, making it an important intermediate in organic synthesis.

Recent studies have highlighted the role of 3-bromoprop-2-en-1-ol in various fields, including pharmaceuticals, agrochemicals, and materials science. Its ability to undergo nucleophilic substitution and elimination reactions has been extensively explored, particularly in the context of developing efficient synthetic pathways for complex molecules. For instance, researchers have utilized 3-bromoprop-2-en-1-ol as a key intermediate in the synthesis of bioactive compounds, such as antibiotics and antiviral agents.

The synthesis of 3-bromoprop-2-en-1-ol typically involves the reaction of allyl alcohol with bromine in the presence of a suitable catalyst. This process is highly controlled to ensure the formation of the desired enantiomer, which is crucial for applications in asymmetric synthesis. The compound's reactivity is further enhanced by its ability to form stable intermediates under specific reaction conditions, making it a valuable tool in modern organic chemistry.

In terms of applications, 3-bromoprop-2-en-1-ol has been employed in the preparation of advanced materials, such as polymers and surfactants. Its unique properties allow for the creation of materials with tailored functionalities, including improved biocompatibility and environmental degradation profiles. For example, recent research has demonstrated the use of 3-bromoprop-2-en-1-ol in the development of biodegradable polymers for biomedical applications.

The compound's stability and reactivity make it an ideal candidate for use in both laboratory and industrial settings. Its compatibility with various reaction conditions ensures that it can be integrated into diverse synthetic workflows without compromising product quality or yield. Furthermore, the availability of high-purity 3-bromoprop-2-en-1 ol from reputable suppliers has facilitated its widespread adoption across multiple industries.

From an environmental perspective, the use of 3-bromopropenyl alcohol (another name for this compound) has been scrutinized due to its potential impact on ecosystems. However, advancements in green chemistry have led to the development of more sustainable production methods and application techniques that minimize environmental risks while maintaining product efficacy.

In conclusion, 3-bromopropenyl alcohol (CAS No. 37675 0) remains a critical compound in contemporary organic chemistry due to its unique properties and versatility across multiple applications. As research continues to uncover new uses and optimizations for this compound, its role in driving innovation across various industries is expected to grow significantly.

• 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)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 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)