Date published: 2026-5-19

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Tris(4-bromophenyl)ammoniumyl hexachloroantimonate (CAS 24964-91-8)

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CAS Number:
24964-91-8
Molecular Weight:
816.48
Molecular Formula:
C18H12Br3Cl6NSb
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Tris(4-bromophenyl)ammoniumyl hexachloroantimonate functions as a catalyst in organic synthesis, functioning in the formation of carbon-carbon and carbon-heteroatom bonds. Its mechanism of action involves facilitating the coupling of organic substrates through a series of chemical reactions, leading to the formation of new chemical compounds. Tris(4-Bromophenyl)Ammoniumyl Hexachloroantimonate acts as a Lewis acid, promoting the activation of organic molecules and enabling them to undergo various transformations. Through its interaction with the reactants, it enhances the efficiency of the process by lowering the activation energy and promoting the desired chemical reactions. Tris(4-bromophenyl)ammoniumyl hexachloroantimonate plays a role in the development of new organic compounds and materials by enabling the construction of complex molecular structures through controlled chemical reactions. Its ability to catalyze specific bond-forming reactions may be a function in the exploration of novel chemical pathways and the synthesis of diverse organic compounds.


Tris(4-bromophenyl)ammoniumyl hexachloroantimonate (CAS 24964-91-8) References

  1. Glycosylation using a one-electron-transfer, homogeneous reagent. Application to an efficient synthesis of the trimannosyl core of N-glycosylproteins.  |  Zhang, YM., et al. 1992. Carbohydr Res. 236: 73-88. PMID: 1291063
  2. Structural, spectroscopic, and computational study of an octahedral, non-heme [Fe-NO](6-8) Series: [Fe(NO)(cyclam-ac)]2+/+/0.  |  Serres, RG., et al. 2004. J Am Chem Soc. 126: 5138-53. PMID: 15099097
  3. Characterization and reactivity of a terminal nickel(III)-oxygen adduct.  |  Pirovano, P., et al. 2015. Chemistry. 21: 3785-90. PMID: 25612563
  4. Tuning the Reactivity of Terminal Nickel(III)-Oxygen Adducts for C-H Bond Activation.  |  Pirovano, P., et al. 2016. J Am Chem Soc. 138: 14362-14370. PMID: 27739688
  5. Tris(4-bromophenyl)aminium Hexachloroantimonate-Initiated Oxidative Povarov-Type Reaction between Glycine Esters and (Cyclopropylidenemethyl)benzenes Using the Counterion as a Chlorine Donor.  |  Yuan, Y., et al. 2020. Org Lett. 22: 6294-6298. PMID: 32806190
  6. Aminium cation-radical catalysed selective hydration of (E)-aryl enynes.  |  Giel, MC., et al. 2021. Chem Commun (Camb). 57: 6991-6994. PMID: 34159967
  7. Tris(4-bromophenyl)aminium Hexachloroantimonate as a 'Waste-Utilized'-Type Initiator-Promoted C-H Chlorination via C-H Activation Relay: Synthesis of Chlorinated Pyrroles.  |  Ding, H., et al. 2022. J Org Chem. 87: 15139-15151. PMID: 36398528
  8. Synthesis, Hole Doping, and Electrical Properties of a Semiconducting Azatriangulene-Based Covalent Organic Framework.  |  Burke, DW., et al. 2023. J Am Chem Soc. 145: 11969-11977. PMID: 37216443

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Tris(4-bromophenyl)ammoniumyl hexachloroantimonate, 1 g

sc-251397
1 g
$28.00