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Key Documents

308285

Sigma-Aldrich

Indium(III) bromide

99%

Synonym(s):

Indium tribromide

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About This Item

Linear Formula:
InBr3
CAS Number:
Molecular Weight:
354.53
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.23

vapor density

>1 (vs air)

Assay

99%

form

powder and chunks

reaction suitability

reagent type: catalyst
core: indium

bp

656 °C (lit.)

mp

436 °C (lit.)

density

4.96 g/mL at 25 °C (lit.)

SMILES string

Br[In](Br)Br

InChI

1S/3BrH.In/h3*1H;/q;;;+3/p-3

InChI key

JKNHZOAONLKYQL-UHFFFAOYSA-K

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Application


  • Investigation of the Solution Chemistry of Hybrid Organic–Inorganic Indium Halides for New Material Discovery: The study examines the indium(III) bromide system, MA–In–Br, and the formation of new indium(III) halides (Zhang et al., 2022).

  • Indium (III)‐Catalyzed Haloalkynylation Reaction of Alkynes: This research explores the use of indium(III) bromide as a catalyst in haloalkynylation reactions (Daniels et al., 2024).

  • Zero-Dimensional Hybrid Organic–Inorganic Indium Bromide with Blue Emission: The study reports on the synthesis and properties of a new indium bromide compound exhibiting blue emission (Fattal et al., 2021).

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Karavadhi Surendra et al.
Journal of the American Chemical Society, 133(25), 9724-9726 (2011-06-08)
InI(3) and InBr(3) have been found to be effective catalysts for the π activation of C≡C bonds to initiate the conversion of chiral propargylic alcohols or silyl ethers to polycyclic products in excellent yields and with high stereoselectivity. The method

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