Date published: 2026-4-5

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Indium(I) bromide (CAS 14280-53-6)

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CAS Number:
14280-53-6
Molecular Weight:
194.72
Molecular Formula:
InBr
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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Indium(I) bromide is widely used in research primarily focused on material science and organic synthesis. This compound is valuable for its role in the synthesis of complex organic molecules, acting as a catalyst or reagent that facilitates various chemical transformations. Researchers utilize Indium(I) bromide to study its effectiveness in promoting allylation reactions, which are for forming carbon-carbon bonds in organic compounds. Additionally, it is employed in the deposition processes of thin films for electronic and photonic devices, where its properties help in the development of indium-containing layers. The research involving Indium(I) bromide significantly advances the understanding of its chemical behavior and potential applications in creating advanced materials and chemicals.


Indium(I) bromide (CAS 14280-53-6) References

  1. Reactions of Elemental Indium and Indium(I) Bromide with Nickel-Bromine Bonds: Structure of (eta(5)-C(5)H(5))(Ph(3)P)Ni-InBr(2)(O=PPh(3)).  |  Weiss, J., et al. 1996. Inorg Chem. 35: 71-75. PMID: 11666166
  2. A new route to 2-C- and 4-C-branched sugars by palladium-indium bromide-mediated carbonyl allylation.  |  Norsikian, S. and Lubineau, A. 2005. Org Biomol Chem. 3: 4089-94. PMID: 16267588
  3. Ruthenium(III)-catalysed phenylselenylation of allyl acetates by diphenyl diselenide and indium(I) bromide in neat: isolation and identification of intermediate.  |  Saha, A. and Ranu, BC. 2011. Org Biomol Chem. 9: 1763-7. PMID: 21258726
  4. Reactions of Elemental Indium and Indium(I) Bromide with Nickel−Bromine Bonds:  Structure of (η5-C5H5)(Ph3P)NiInBr2(OPPh3)†  |  Jurij Weiss, Thomas Priermeier, and Roland A. Fischer. 1996. Inorg. Chem., 35, 1,: 71–75.
  5. Indium(I) bromide-mediated coupling of dibromoacetonitrile with aldehydes followed by Boord elimination of bromine and oxygen of β-bromo alkoxides for preparation of 3-organyl-2-alkenenitriles  |  Clovis Peppe, Paola de Azevedo Mello, Rafael Pavão das Chagas. 15 May 2006,. Journal of Organometallic Chemistry. Volume 691, Issue 11,: Pages 2335-2339.
  6. Indium(I) bromide-promoted stereoselective preparation of cyclopropanes via sequential aldol-type coupling/elimination/Michael-induced ring closure reaction from α,α-dichloroacetophenone and aldehydes  |  Clovis Peppe, Rafael Pavão das Chagas, Robert Alan Burrow. 15 October 2008,. Journal of Organometallic Chemistry. Volume 693, Issues 21–22,: Pages 3441-3445.
  7. Indium (I) bromide-mediated dichlorocyanomethylation of carbonyl compounds. The preparation of 2, 2-dichloro-3-hydroxynitriles  |  J.A Nóbrega a, Simone M.C Gonçalves a, C Peppe b. 16 July 2001,. Tetrahedron Letters. Volume 42, Issue 29,: Pages 4745-4746.
  8. The high temperature heat capacities of indium(i) bromide and indium(III) bromide by differential scanning calorimetry  |  Peter J. Gardner, Steve R. Preston. 26 April 1991,. Thermochimica Acta. Volume 180,: Pages 281-287.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Indium(I) bromide, 5 g

sc-257603
5 g
$212.00