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Merck
모든 사진(2)

문서

224839

Sigma-Aldrich

Bismuth(III) chloride

reagent grade, ≥98%

동의어(들):

Bismuth trichloride, Trichlorobismuth

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About This Item

실험식(Hill 표기법):
BiCl3
CAS Number:
Molecular Weight:
315.34
EC Number:
MDL number:
UNSPSC 코드:
12352302
PubChem Substance ID:
NACRES:
NA.21

Grade

reagent grade

Quality Level

분석

≥98%

형태

powder, chunks or granules

반응 적합성

reagent type: catalyst
core: bismuth

bp

447 °C (lit.)

mp

230-232 °C (lit.)

SMILES string

Cl[Bi](Cl)Cl

InChI

1S/Bi.3ClH/h;3*1H/q+3;;;/p-3

InChI key

JHXKRIRFYBPWGE-UHFFFAOYSA-K

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일반 설명

Bismuth(III) chloride is an inorganic salt that can be prepared by the reaction of bismuth with chlorine.

애플리케이션

Bismuth(III) chloride may be used as a catalyst in the following processes:
  • Alcoholysis, acetolysis and hydrolysis of epoxides to form the corresponding β-alkoxy and β-acetoxy alcohols and diols.
  • Preparation of thiiranes from oxiranes using ammonium thiocyanate.
  • Three component coupling of carbonyl compound, amine and dialkyl phosphite to form α-amino phosphonates.
  • Allylation of secondary benzyl alcohols with allyltrimethylsilane.
  • [4 + 2] cycloaddition between dienes and α-carbonyl ethylenic dienophiles.

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


시험 성적서(COA)

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문서 라이브러리 방문

Daintith J
The facts on file dictionary of chemistry, 28-28 (2014)
Bismuth (III) chloride-catalyzed direct deoxygenative allylation of substituted benzylic alcohols with allyltrimethylsilane
De SK & Gibbs RA.
Tetrahedron Letters, 46(48), 8345-8350 (2005)
Bismuth (III) chloride (BiCl3)-An efficient catalyst for mild, regio-and stereoselective cleavage of epoxides with alcohols, acetic Acid and water.
Mohammadpoor-Baltork I.
Synthetic Communications, 30(13), 2365-2374 (2000)
Bismuth (III) Chloride-Catalyzed Three-Component Coupling: Synthesis of a-Amino Phosphonates.
Zhan ZP and Li JP.
Synthetic Communications, 35(19), 2501-2508 (2005)
Bismuth (iii) Chloride Mediated Michaelis-Arbuzov Reaction: A Facile Synthesis of Substituted Arylphosphonates/Phosphinates and Bioactivity Evaluation.
Subramanyam C, et al.
Phosph. Sulfur Relat. Elem. (2015)

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