Cas no 16604-98-1 (2-Chloro-5-Iodoaniline)
2-Chloro-5-Iodoaniline Chemical and Physical Properties
Names and Identifiers
-
- 2-Chlor-5-iodanilin
- 2-Chlor-5-iod-anilin
- 2-Chlor-5-jod-anilin
- 2-chloro-5-iodo-aniline
- 2-CHLORO-5-IODOPHENYLAMINE
- AB64100
- AC1Q5108
- AG-E-15608
- CTK4D2234
- SureCN1932575
- 2-chloro-5-iodoaniline
- Benzenamine, 2-chloro-5-iodo-
- 16604-98-1
- PSXCVXYHPJLMGU-UHFFFAOYSA-N
- J-010252
- Z414834738
- SCHEMBL1932575
- DTXSID30653866
- F83085
- DB-217222
- CS-0217844
- EN300-88616
- AKOS027326278
- 2-Chloro-5-Iodoaniline
-
- MDL: MFCD11505641
- Inchi: 1S/C6H5ClIN/c7-5-2-1-4(8)3-6(5)9/h1-3H,9H2
- InChI Key: PSXCVXYHPJLMGU-UHFFFAOYSA-N
- SMILES: IC1=CC=C(C(=C1)N)Cl
Computed Properties
- Exact Mass: 252.91552g/mol
- Monoisotopic Mass: 252.91552g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 9
- Rotatable Bond Count: 0
- Complexity: 99.1
- 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: 2.8
- Topological Polar Surface Area: 26?2
2-Chloro-5-Iodoaniline Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A013027279-250mg |
2-Chloro-5-iodoaniline |
16604-98-1 | 97% | 250mg |
504.00 USD | 2021-06-22 | |
| Alichem | A013027279-500mg |
2-Chloro-5-iodoaniline |
16604-98-1 | 97% | 500mg |
806.85 USD | 2021-06-22 | |
| Alichem | A013027279-1g |
2-Chloro-5-iodoaniline |
16604-98-1 | 97% | 1g |
1,564.50 USD | 2021-06-22 | |
| TRC | C386448-25mg |
2-Chloro-5-Iodoaniline |
16604-98-1 | 25mg |
$ 50.00 | 2022-06-06 | ||
| TRC | C386448-50mg |
2-Chloro-5-Iodoaniline |
16604-98-1 | 50mg |
$ 95.00 | 2022-06-06 | ||
| TRC | C386448-250mg |
2-Chloro-5-Iodoaniline |
16604-98-1 | 250mg |
$ 320.00 | 2022-06-06 | ||
| Enamine | EN300-88616-0.05g |
2-chloro-5-iodoaniline |
16604-98-1 | 95% | 0.05g |
$66.0 | 2023-09-01 | |
| Enamine | EN300-88616-0.1g |
2-chloro-5-iodoaniline |
16604-98-1 | 95% | 0.1g |
$98.0 | 2023-09-01 | |
| Enamine | EN300-88616-0.25g |
2-chloro-5-iodoaniline |
16604-98-1 | 95% | 0.25g |
$142.0 | 2023-09-01 | |
| Enamine | EN300-88616-0.5g |
2-chloro-5-iodoaniline |
16604-98-1 | 95% | 0.5g |
$271.0 | 2023-09-01 |
2-Chloro-5-Iodoaniline Related Literature
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H. V. Jain,D. Verthelyi,S. L. Beaucage RSC Adv., 2017,7, 42519-42528
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Andre Prates Pereira,Tao Dong,Eric P. Knoshaug,Nick Nagle,Ryan Spiller,Bonnie Panczak,Christopher J. Chuck,Philip T. Pienkos Sustainable Energy Fuels, 2020,4, 3400-3408
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Bidyut Kumar Kundu,Rinky Singh,Ritudhwaj Tiwari,Debasis Nayak New J. Chem., 2019,43, 4867-4877
-
Chengbin Yang,Hing Lun Tsang,Pui Man Lau,Ken-Tye Yong,Ho Pui Ho,Siu Kai Kong Analyst, 2017,142, 3579-3587
Additional information on 2-Chloro-5-Iodoaniline
2-Chloro-5-Iodoaniline: A Comprehensive Overview
2-Chloro-5-Iodoaniline, also known by its CAS registry number CAS No. 16604-98-1, is a significant compound in the field of organic chemistry. This compound has garnered attention due to its unique properties and potential applications in various industries. In this article, we will delve into the structural characteristics, chemical properties, synthesis methods, and recent advancements in its applications.
The molecular structure of 2-Chloro-5-Iodoaniline consists of an aniline backbone with a chlorine atom at the second position and an iodine atom at the fifth position. This substitution pattern imparts distinct electronic and steric properties to the molecule, making it versatile for different chemical reactions. Recent studies have highlighted its role as an intermediate in the synthesis of complex aromatic compounds, particularly in the pharmaceutical and agrochemical sectors.
One of the most notable aspects of 2-Chloro-5-Iodoaniline is its reactivity under various conditions. Research conducted in 2023 has shown that this compound can undergo nucleophilic aromatic substitution efficiently when activated by appropriate directing groups. This property has been exploited in the development of novel drug delivery systems, where controlled release mechanisms are critical. Additionally, its ability to act as a precursor for bioactive molecules has positioned it as a key player in medicinal chemistry.
The synthesis of 2-Chloro-5-Iodoaniline typically involves multi-step processes, including chlorination and iodination reactions. Recent advancements have focused on optimizing these steps to enhance yield and reduce environmental impact. For instance, catalytic methods using transition metal catalysts have been reported to significantly improve reaction efficiency while minimizing by-products.
In terms of applications, 2-Chloro-5-Iodoaniline has found utility in the production of advanced materials such as conductive polymers and high-performance composites. Its role as a building block for these materials is supported by its ability to form stable covalent bonds under thermal or photochemical conditions. Furthermore, ongoing research is exploring its potential in energy storage technologies, where its electronic properties could contribute to more efficient battery systems.
Safety considerations are paramount when handling 2-Chloro-5-Iodoaniline. While it is not classified as a hazardous material under standard conditions, proper precautions should be taken to avoid exposure during synthesis and handling. Recent guidelines emphasize the importance of using personal protective equipment and ensuring adequate ventilation in laboratory settings.
In conclusion, 2-Chloro-5-Iodoaniline, with its CAS number CAS No. 16604-98-1, continues to be a focal point in chemical research due to its unique properties and diverse applications. As new discoveries emerge, this compound is expected to play an even more pivotal role in advancing various scientific fields.
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