Cas no 38380-55-1 (8-Iodooct-1-ene)
8-Iodooct-1-ene Chemical and Physical Properties
Names and Identifiers
-
- 1-Octene, 8-iodo-
- 8-iodooct-1-ene
- DTXSID50551911
- CS-0036274
- 1-iodo-7-octene
- MFCD28991915
- 38380-55-1
- AS-56914
- SY126684
- SCHEMBL757970
- W11175
- AKOS037645083
- 8-iodo-oct-1-ene
- XBRJYHWTXTYAOC-UHFFFAOYSA-N
- 8-Iodooct-1-ene, stabilized over Cu
- EN300-20984841
- 8-iodo-1-octene
- 8-Iodooct-1-ene
-
- MDL: MFCD28991915
- Inchi: 1S/C8H15I/c1-2-3-4-5-6-7-8-9/h2H,1,3-8H2
- InChI Key: XBRJYHWTXTYAOC-UHFFFAOYSA-N
- SMILES: ICCCCCCC=C
Computed Properties
- Exact Mass: 238.02145
- Monoisotopic Mass: 238.02185g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 0
- Heavy Atom Count: 9
- Rotatable Bond Count: 6
- Complexity: 59.6
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 5.4
- Topological Polar Surface Area: 0?2
Experimental Properties
- PSA: 0
8-Iodooct-1-ene Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | I707228-10mg |
8-Iodooct-1-ene |
38380-55-1 | 10mg |
$ 70.00 | 2022-06-04 | ||
| TRC | I707228-50mg |
8-Iodooct-1-ene |
38380-55-1 | 50mg |
$ 230.00 | 2022-06-04 | ||
| TRC | I707228-100mg |
8-Iodooct-1-ene |
38380-55-1 | 100mg |
$ 340.00 | 2022-06-04 | ||
| Enamine | EN300-20984841-1g |
8-iodooct-1-ene |
38380-55-1 | 95% | 1g |
$800.0 | 2023-09-16 | |
| Enamine | EN300-20984841-5g |
8-iodooct-1-ene |
38380-55-1 | 95% | 5g |
$2318.0 | 2023-09-16 | |
| Enamine | EN300-20984841-10g |
8-iodooct-1-ene |
38380-55-1 | 95% | 10g |
$3438.0 | 2023-09-16 | |
| eNovation Chemicals LLC | D772407-100mg |
1-Octene, 8-iodo- |
38380-55-1 | 95% | 100mg |
$265 | 2024-06-06 | |
| eNovation Chemicals LLC | D772407-250mg |
1-Octene, 8-iodo- |
38380-55-1 | 95% | 250mg |
$465 | 2024-06-06 | |
| eNovation Chemicals LLC | D772407-1g |
1-Octene, 8-iodo- |
38380-55-1 | 95% | 1g |
$905 | 2024-06-06 | |
| eNovation Chemicals LLC | D772407-5g |
1-Octene, 8-iodo- |
38380-55-1 | 95% | 5g |
$2715 | 2024-06-06 |
8-Iodooct-1-ene Related Literature
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Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
-
Huading Zhang,Lee R. Moore,Maciej Zborowski,P. Stephen Williams,Shlomo Margel,Jeffrey J. Chalmers Analyst, 2005,130, 514-527
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Tao Wang,Yangyang Liu,Yue Deng,Hongbo Fu,Jianmin Chen Environ. Sci.: Nano, 2018,5, 1821-1833
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Liao Xiaoqing,Li Ruiyi,Li Zaijun,Sun Xiulan,Wang Zhouping,Liu Junkang New J. Chem., 2015,39, 5240-5248
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Aloke Das,K. K. Mahato,Chayan K. Nandi,Tapas Chakraborty,Shridhar R. Gadre,Nikhil A. Gokhale Phys. Chem. Chem. Phys., 2002,4, 2162-2168
Additional information on 8-Iodooct-1-ene
8-Iodooct-1-ene (CAS No. 38380-55-1): A Comprehensive Overview
8-Iodooct-1-ene (CAS No. 38380-55-1) is a versatile organic compound that has garnered significant attention in the fields of organic synthesis, materials science, and pharmacology. This compound, characterized by its iodoalkene structure, exhibits unique chemical properties that make it an invaluable building block in modern chemistry. Recent advancements in synthetic methodologies have further enhanced its utility, positioning it as a key player in the development of novel materials and therapeutic agents.
The structure of 8-Iodooct-1-ene consists of an eight-carbon chain with a double bond at the 1-position and an iodine atom at the terminal end. This configuration imparts the molecule with reactivity that is both predictable and controllable, making it amenable to a wide range of transformations. The iodoalkene functionality is particularly advantageous due to its ability to participate in cross-coupling reactions, which are pivotal in constructing complex molecular architectures.
Recent studies have highlighted the role of 8-Iodooct-1-ene in the synthesis of advanced polymers and biomaterials. Researchers have demonstrated that this compound can serve as a precursor for the generation of highly functionalized polymers with tailored mechanical and electronic properties. For instance, its use in the preparation of conjugated polymers has opened new avenues for applications in organic electronics, such as light-emitting diodes (LEDs) and photovoltaic devices.
In the realm of medicinal chemistry, 8-Iodooct-1-ene has been employed as an intermediate in the synthesis of bioactive molecules. Its ability to undergo metathesis reactions has facilitated the construction of intricate molecular frameworks that mimic natural products. These efforts have contributed to the discovery of potential drug candidates with anti-inflammatory, anticancer, and antimicrobial activities.
The synthesis of 8-Iodooct-1-ene typically involves a combination of traditional organic chemistry techniques and modern catalytic methods. Recent advancements in catalysis, particularly the use of transition metal catalysts, have streamlined its production process, ensuring higher yields and improved purity. This has made 8-Iodooct-1-ene more accessible for both academic research and industrial applications.
From a sustainability perspective, the use of 8-Iodooct-1-ene aligns with green chemistry principles due to its potential for recycling and reusability in certain reaction pathways. Its compatibility with eco-friendly solvents and energy-efficient reaction conditions further underscores its role as a sustainable chemical building block.
In conclusion, 8-Iodooct-1-ene (CAS No. 38380-55-1) stands out as a multifaceted compound with immense potential across diverse scientific disciplines. Its unique chemical properties, combined with cutting-edge research advancements, ensure that it will continue to play a pivotal role in shaping future innovations in chemistry and materials science.
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