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About This Item
Linear Formula:
(CH3)2AlCl
CAS Number:
Molecular Weight:
92.50
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22
form
liquid
concentration
1.0 M in hexanes
density
0.701 g/mL at 25 °C
SMILES string
C[Al](C)Cl
InChI
1S/2CH3.Al.ClH/h2*1H3;;1H/q;;+1;/p-1
InChI key
JGHYBJVUQGTEEB-UHFFFAOYSA-M
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General description
Dimethylaluminum chloride (Me2AlCl) is a mild Lewis acid and acts as a proton scavenger. It catalyzes living isobutylene polymerization. Exceptional chelating potential of Me2AlCl, and its companion Lewis acid MeAlCl2, for the chelate-organized carbonyl addition reactions has been investigated. It effectively promotes chelate-controlled aldol and related allylsilane additions.
Application
Dimethylaluminum chloride may be employed as catalyst for the ene reaction of aliphatic and aromatic aldehydes with alkenes having a disubstituted vinylic carbon.
Signal Word
Danger
Hazard Statements
Hazard Classifications
Aquatic Chronic 2 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 2 - Pyr. Liq. 1 - Repr. 2 - Skin Corr. 1B - STOT RE 1 Inhalation - STOT SE 3 - Water-react 1
Target Organs
Central nervous system, Nervous system
Storage Class Code
4.2 - Pyrophoric and self-heating hazardous materials
WGK
WGK 3
Flash Point(F)
-9.4 °F
Flash Point(C)
-23 °C
Regulatory Information
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D A Evans et al.
Journal of the American Chemical Society, 123(44), 10840-10852 (2001-11-01)
A systematic investigation of the stereoselectivity in Lewis acid-promoted (Mukaiyama) aldol reactions of achiral unsubstituted enolsilanes and chiral beta-hydroxy aldehydes proceeding under conditions favoring chelation control is presented. Good stereocontrol can be realized for enolsilane aldol reactions of beta-alkoxy and
Dimethylaluminum chloride catalyzed ene reactions of aldehydes.
Snider BB, et al.
Journal of the American Chemical Society, 104(2), 555-563 (1982)
Dimethylaluminum chloride catalyzed living isobutylene polymerization.
Bahadur M, et al.
Macromolecules, 33(26), 9548-9552 (2000)
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