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249882

Sigma-Aldrich

Aluminum chloride solution

1.0 M in nitrobenzene

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About This Item

Empirical Formula (Hill Notation):
AlCl3
CAS Number:
7446-70-0
Molecular Weight:
133.34
MDL number:
MFCD00003422
UNSPSC Code:
12352302
PubChem Substance ID:
329752764
NACRES:
NA.55

form

liquid

Quality Level

100

reaction suitability

reagent type: catalyst
core: aluminum

concentration

0.95-1.10 M (EDTA titration)
1.0 M in nitrobenzene

density

1.249 g/mL at 25 °C

SMILES string

Cl[Al](Cl)Cl

InChI

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

InChI key

VSCWAEJMTAWNJL-UHFFFAOYSA-K

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Related Categories

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - Carc. 2 - Eye Dam. 1 - Repr. 1B - Skin Corr. 1B - STOT RE 1 Inhalation

Target Organs

Blood

Supplementary Hazards

EUH014,EUH071

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

190.4 °F - closed cup

Flash Point(C)

88 °C - closed cup

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Acceleration of the Diels-Alder reaction by aluminum chloride.
Yates P and Eaton P.
Journal of the American Chemical Society, 82(16), 4426-4437 (1960)
Amination of< i> exo</i>-2-chloronorbornane and norbornane with trichloramine-aluminum chloride.
Kovacic P, et al.
Tetrahedron, 26(2), 529-538 (1970)
Zhiliang Huang et al.
Organic & biomolecular chemistry, 11(11), 1810-1814 (2013-02-08)
AlCl(3) promoted Friedel-Crafts acylation between 4-tert-butylbenzoyl chloride and mesitylene was investigated. The donor-acceptor complex was observed as the major species. Kinetic investigation demonstrated that the reaction was first-order on the donor-acceptor complex and zero-order on ArH, suggesting that the donor-acceptor
Bagineni Prasad et al.
Chemical communications (Cambridge, England), 48(84), 10434-10436 (2012-09-20)
A conceptually new and straightforward introduction of sulfonyl groups at the C-7 position of an indole ring has been achieved via AlCl(3) mediated unexpected regioselective sulfonyl group migration for N-alkyl/aryl/heteroarylsulfonyl indoles affording potential inhibitors of Mycobacterium tuberculosis H37Rv chorismate mutase.
Mengyun Zhu et al.
Organic letters, 16(7), 1856-1859 (2014-03-19)
An unprecedented AlCl3-promoted formal [2 + 3]-cycloaddition of 1,1-cyclopropanes with readily available N-benzylic sulfonamides has been developed. Experimental evidence supports an unusual mechanism wherein the donor-acceptor cyclopropane serves as a source of 2-styrylmalonate rather than the "classical" 1,3-dipole. A broad
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