Cas no 1806983-87-8 (2,4-Bis(trifluoromethyl)-5-bromobenzenesulfonyl chloride)
2,4-Bis(trifluoromethyl)-5-bromobenzenesulfonyl chloride is a highly reactive sulfonyl chloride derivative, primarily used as a versatile intermediate in organic synthesis and pharmaceutical applications. Its key structural features include two electron-withdrawing trifluoromethyl groups and a bromine substituent, which enhance its reactivity in nucleophilic substitution and cross-coupling reactions. The sulfonyl chloride moiety facilitates the introduction of sulfonamide or sulfonate functionalities, making it valuable for constructing complex molecules. Its stability under controlled conditions and compatibility with a range of reagents underscore its utility in fine chemical synthesis. This compound is particularly suited for applications requiring selective functionalization in trifluoromethyl-substituted aromatic systems.
1806983-87-8 structure
Product Name:2,4-Bis(trifluoromethyl)-5-bromobenzenesulfonyl chloride
CAS No:1806983-87-8
MF:C8H2BrClF6O2S
MW:391.512700557709
CID:4971097
Update Time:2025-10-15
2,4-Bis(trifluoromethyl)-5-bromobenzenesulfonyl chloride Chemical and Physical Properties
Names and Identifiers
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- 2,4-Bis(trifluoromethyl)-5-bromobenzenesulfonyl chloride
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- Inchi: 1S/C8H2BrClF6O2S/c9-5-2-6(19(10,17)18)4(8(14,15)16)1-3(5)7(11,12)13/h1-2H
- InChI Key: SVXVCOODSDQYOQ-UHFFFAOYSA-N
- SMILES: BrC1=CC(=C(C(F)(F)F)C=C1C(F)(F)F)S(=O)(=O)Cl
Computed Properties
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 8
- Heavy Atom Count: 19
- Rotatable Bond Count: 1
- Complexity: 428
- XLogP3: 4.4
- Topological Polar Surface Area: 42.5
2,4-Bis(trifluoromethyl)-5-bromobenzenesulfonyl chloride Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A013024913-1g |
2,4-Bis(trifluoromethyl)-5-bromobenzenesulfonyl chloride |
1806983-87-8 | 97% | 1g |
1,490.00 USD | 2021-06-24 |
2,4-Bis(trifluoromethyl)-5-bromobenzenesulfonyl chloride Related Literature
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Bidyut Kumar Kundu,Rinky Singh,Ritudhwaj Tiwari,Debasis Nayak New J. Chem., 2019,43, 4867-4877
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Juan J. Sánchez,Miguel López-Haro,Juan C. Hernández-Garrido,Ginesa Blanco,Miguel A. Cauqui,José M. Rodríguez-Izquierdo,José A. Pérez-Omil,José J. Calvino,María P. Yeste J. Mater. Chem. A, 2019,7, 8993-9003
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Jieun Kim,Han-Saem Park,Tae-Hee Kim,Sung Yeol Kim,Hyun-Kon Song Phys. Chem. Chem. Phys., 2014,16, 5295-5300
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Inês S. Albuquerque,Hélia F. Jeremias,Miguel Chaves-Ferreira,Dijana Matak-Vinkovic,Omar Boutureira,Carlos C. Rom?o Chem. Commun., 2015,51, 3993-3996
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