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7787-60-2 - Bismuth(III) chloride, 98% (dry wt.), may cont. up to 3% water - A10510 - Alfa Aesar

A10510 Bismuth(III) chloride, 98% (dry wt.), may cont. up to 3% water

Numéro CAS
7787-60-2
Synonymes

Dimensions Prix ($) Quantité Disponibilité
25g 45,70
100g 122,00
500g 498,00
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Bismuth(III) chloride, 98% (dry wt.), may cont. up to 3% water

MDL
MFCD00003461
EINECS
232-123-2

Propriétés chimiques

Formule
BiCl3
Poids formulaire
315.34
Point de fusion
230-232°
Point d'ébullition
ca 430° subl.
Densité
4.75
Sensibilité
Hygroscopic
Solubilité
Soluble in hydrochloric acid, nitric acid, diethyl ether, ethyl acetate and acetone. Insoluble in alcohol.

Applications

Bismuth(III) chloride is used as a catalyst in organic synthesis and to prepare other bismuth salts. It is used as a starting material for the preparation of bismuthoxychloride upon hydrolysis. It is an oxidizing agent to prepare metallic bismuth by reducing agent. Further, it catalyzes the Michael reaction and the Mukaiyama-aldol reaction. In addition to this, it is a Lewis acid.

Notes

Hygroscopic. Incompatible with strong oxidizing agents.

Références bibliographiques

Lewis acid catalyst which promotes the rearrangement of acetanilides to o-amino ketones: Tetrahedron Lett., 3217 (1976).

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).

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).

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).

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).

Antonio, M. R.; McAlister, D. R.; Horwitz, E. P. An europium(III) diglycolamide complex: insights into the coordination chemistry of lanthanides in solvent extraction. Dalton Trans. 2015, 44 (2), 515-521.

Vuorinen, S.; Lahcini, M.; Hatanpää, T.; Sundberg, M.; Leskelä, M.; Repo, T. Bismuth(III) Alkoxide Catalysts for Ring-Opening Polymerization of Lactides and ε-Caprolactone. Macromol. Chem. Phys. 2013, 214 (6), 707-715.

Mentions de danger et de prudence du SGH

Mentions de danger (UE): H314-H318-H303

Causes severe skin burns and eye damage. Causes serious eye damage. May be harmful if swallowed.

Mentions de prudence: P260-P280-P303+P361+P353-P305+P351+P338-P301+P330+P331-P304+P340-P310-P312-P405-P501a

Do not breathe dust/fume/gas/mist/vapours/spray. Wear protective gloves/protective clothing/eye protection/face protection. IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Immediately call a POISON CENTER or doctor/physician. Call a POISON CENTER or doctor/physician if you feel unwell. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.

Autres références

Merck
14,1262
Classe de danger
8
Groupe d'emballage
III
Code tarifaire harmonisé
2827.39
TSCA
Yes
RTECS
EB2690000

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