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安全信息

248843

Sigma-Aldrich

二甲基氯化铝 溶液

1.0 M in hexanes

别名:

Chlorodimethylaluminum, Dimethylaluminum chloride, Dimethylchloralane, Dimethylchloroalane, Dimethylchloroaluminum

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About This Item

线性分子式:
(CH3)2AlCl
CAS号:
1184-58-3
分子量:
92.50
MDL编号:
MFCD00000458
UNSPSC代码:
12352103
PubChem化学物质编号:
24854954
NACRES:
NA.22

表单

liquid

浓度

1.0 M in hexanes

密度

0.701 g/mL at 25 °C

SMILES字符串

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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一般描述

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.

应用

Dimethylaluminum chloride may be employed as catalyst for the ene reaction of aliphatic and aromatic aldehydes with alkenes having a disubstituted vinylic carbon.

警示用语：

Danger

危险分类

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

靶器官

Central nervous system, Nervous system

储存分类代码

4.2 - Pyrophoric and self-heating hazardous materials

WGK

WGK 3

闪点(°F)

-9.4 °F

闪点(°C)

-23 °C

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
STBJ5219
STBH3034
STBF8979V
STBF4872V
STBC9422V

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Dimethylaluminum chloride catalyzed living isobutylene polymerization.
Bahadur M, et al.
Macromolecules, 33(26), 9548-9552 (2000)
Dimethylaluminum chloride catalyzed ene reactions of aldehydes.
Snider BB, et al.
Journal of the American Chemical Society, 104(2), 555-563 (1982)
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

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