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Bismuth(III) chloride_Molecular_structure_CAS_7787-60-2)
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Bismuth(III) chloride

Catalog No. A10510 Name Alfa Aesar
CAS Number 7787-60-2 Website
M. F. BiCl3 Telephone
M. W. 315.3394 Fax
Purity 98% (dry wt.), may cont. up to 3% water Email
Storage Chembase ID: 295163

SYNONYMS

Title
氯化铋(III)
IUPAC name
bismuth(3+) ion trichloride
IUPAC Traditional name
bismuth(3+) ion trichloride

DATABASE IDS

EC Number 232-123-2
MDL Number MFCD00003461
Merck Index 141262
CAS Number 7787-60-2

PROPERTIES

Purity 98% (dry wt.), may cont. up to 3% water
Boiling Point ca 430°C subl.
Density 4.75
Melting Point 230-232°C
GHS Pictograms GHS05
GHS Hazard statements H314-H318
European Hazard Symbols Corrosive Corrosive (C)
GHS Precautionary statements P260-P303+P361+P353-P305+P351+P338-P301+P330+P331-P405-P501A
Risk Statements 34
RTECS EB2690000
Safety Statements 26-36/37/39-45
Storage Warning Hygroscopic
TSCA Listed
Hazard Class 8
UN Number UN3260
Packing Group III

DETAILS

REFERENCES

  • Promotes the chemoselective deprotection of N-Boc amino acids and peptides: Tetrahedron Lett., 47, 389 (2006).
  • For a brief feature on Bi(III) catalysts, see: Synlett, 1194 (2001). For a review of their use in acylation and sulfonylation reactions, see: Synlett, 181 (2002).
  • Lewis acid catalyst which promotes the rearrangement of acetanilides to o-amino ketones: Tetrahedron Lett., 3217 (1976).
  • Catalyzes the addition of 1,3-dicarbonyl compounds to Michael acceptors under solvent-free conditions with microwave irradiation: Tetrahedron Lett., 38, 1449 (1997).
  • For catalysis of Diels-Alder and hetero Diels-Alder reactions, see: J. Org. Chem., 62, 4880 (1997); Tetrahedron Lett., 39, 1161 (1998).
  • Silyl enol ethers can be ɑ-acylated with acyl chlorides in the presence of a catalytic amount of BiCl3 and NaI or ZnI2; other Lewis acids such as ZnCl2 were less effective: J. Org. Chem., 61, 3885 (1996).
  • Arenes undergo sufonylation by heating with arenesulfonyl chlorides in the presence of BiCl3 (5 mol%) and triflic acid (10 mol%) to give high yields of mixed diaryl sulfones; neither BiCl3 nor TfOH alone is effective: Tetrahedron Lett., 40, 9233 (1999).