Cas no 1806347-41-0 (4,5-Dibromo-2-iodopyridine)
4,5-Dibromo-2-iodopyridine is a halogenated pyridine derivative widely utilized as a versatile intermediate in organic synthesis and pharmaceutical research. Its distinct bromine and iodine substituents enhance reactivity, enabling selective functionalization for constructing complex heterocyclic frameworks. The compound is particularly valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, due to its halogen-rich structure. It also serves as a precursor for agrochemicals and bioactive molecules. High purity grades ensure consistent performance in demanding applications. The stability and well-defined reactivity of 4,5-Dibromo-2-iodopyridine make it a reliable choice for researchers developing advanced materials and fine chemicals. Proper handling under inert conditions is recommended to preserve its integrity.
4,5-Dibromo-2-iodopyridine structure
Product Name:4,5-Dibromo-2-iodopyridine
CAS No:1806347-41-0
MF:C5H2Br2IN
MW:362.788551807404
CID:4802526
Update Time:2025-06-09
4,5-Dibromo-2-iodopyridine Chemical and Physical Properties
Names and Identifiers
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- 4,5-Dibromo-2-iodopyridine
-
- Inchi: 1S/C5H2Br2IN/c6-3-1-5(8)9-2-4(3)7/h1-2H
- InChI Key: BWHOYYRMNWWJEV-UHFFFAOYSA-N
- SMILES: IC1C=C(C(=CN=1)Br)Br
Computed Properties
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 9
- Rotatable Bond Count: 0
- Complexity: 101
- XLogP3: 2.9
- Topological Polar Surface Area: 12.9
4,5-Dibromo-2-iodopyridine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A029007315-250mg |
4,5-Dibromo-2-iodopyridine |
1806347-41-0 | 95% | 250mg |
$1,038.80 | 2022-03-31 | |
| Alichem | A029007315-500mg |
4,5-Dibromo-2-iodopyridine |
1806347-41-0 | 95% | 500mg |
$1,600.75 | 2022-03-31 | |
| Alichem | A029007315-1g |
4,5-Dibromo-2-iodopyridine |
1806347-41-0 | 95% | 1g |
$2,952.90 | 2022-03-31 |
4,5-Dibromo-2-iodopyridine Related Literature
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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
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Marcin Czapla,Jack Simons Phys. Chem. Chem. Phys., 2018,20, 21739-21745
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Vishwesh Venkatraman,Marco Foscato,Vidar R. Jensen,Bj?rn K?re Alsberg J. Mater. Chem. A, 2015,3, 9851-9860
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Hongxia Li,Aikifa Raza,Qiaoyu Ge,Jin-You Lu,TieJun Zhang Soft Matter, 2020,16, 6841-6849
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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
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