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CAS No 13465-09-3 , tribromoindigane Search by region : Germany

  • Name: tribromoindigane
  • Synonyms: tribromoindigane; 13465-09-3; 308285_ALDRICH;tribromoindigane; 545082_ALDRICH; InBr3; Indium bromide (InBr3); Indium(III) bromide; AC1L1AAI;Indium tribromide;
  • CAS Registry Number:
  • Transport: UN3260
  • Melting Point: 220 °C(lit.)
  • Flash Point: °C
  • Boiling Point: 656 °C(lit.)
  • Density: g/cm3
  • Safety Statements:
    Hazard Codes Xi
    Risk Statements 36/37/38
    Safety Statements 26-36
    RIDADR UN3260
    WGK Germany 3
    HazardClass 8
    PackingGroup III
  • Hazard Symbols: Xi: Irritant;
  • Flash Point: °C
  • EINECS: 236-692-8
  • Molecular Weight: 354.53
  • InchiKey: JKNHZOAONLKYQL-UHFFFAOYSA-K
  • InChI: InChI=1S/3BrH.In/h3*1H;/q;;;+3/p-3
  • Risk Statements: 36/37/38
  • Molecular Formula: Br3In
  • Molecular Structure:CAS No:13465-09-3 tribromoindigane

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13465-09-3 INDIUM(III) BROMIDE, ANHYDROUS; (99.999%-IN) PURATREM

  • Germany ABCR GmbH & Co KG [Manufacturer]
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13465-09-3 (0612) INDIUM (III) BROMIDE

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References of tribromoindigane
Title: Indium Tribromide
CAS Registry Number: 13465-09-3
CAS Name: Indium bromide (InBr3)
Molecular Formula: Br3In
Molecular Weight: 354.53
Percent Composition: Br 67.61%, In 32.39%
Line Formula: InBr3
Literature References: Water-stable, green Lewis acid catalyst. Prepn: G. P. Baxter, C. M. Alter, J. Am. Chem. Soc. 55, 1943 (1933). Hydrolysis constants: T. Moeller, ibid. 64, 953 (1942). Raman spectroscopy of aqueous solns: M. A. Marques et al., J. Chem. Soc. Faraday Trans. 86, 3883 (1990). Chemical bonding analysis of binary indium bromides: R. Dronskowski, Inorg. Chem. 33, 6201 (1994). Catalytic applications in organic synthesis: J. S. Yadav, B. V. S. Reddy, Synthesis 2002, 511; eidem et al., Synlett 2003, 396; C. Peppe et al., ibid. 2004, 1723; L. Yin et al., ibid. 1727; Z.-H. Zhang et al., Adv. Synth. Catal. 348, 184 (2006). Review of synthetic applications: Z.-H. Zhang, Synlett 2005, 711-712.
Properties: White crystalline solid.
Use: Regio-, chemo-, and stereoselective Lewis acid catalyst in organic synthesis.