252662
三乙基铝 溶液
1.0 M in hexanes
别名:
三乙铝
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关于此项目
线性分子式:
Al(C2H5)3
化学文摘社编号:
分子量:
114.16
UNSPSC Code:
12352103
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3587229
InChI
1S/3C2H5.Al/c3*1-2;/h3*1H2,2H3;
SMILES string
CC[Al](CC)CC
InChI key
VOITXYVAKOUIBA-UHFFFAOYSA-N
form
liquid
concentration
1.0 M in hexanes
density
0.692 g/mL at 25 °C
Quality Level
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Application
Triethylaluminum solution can be used:
- As a reagent in Alumino-Mannich reaction, where it reacts with iminium ion substrates for which the corresponding Petasis borono-Mannich reaction is unsuccessful.
- In the synthesis of macrocyclic binuclear aluminum complexes with efficient activities toward ring-opening polymerization of ε-caprolactone.
- To promote Claisen rearrangement of allyl vinyl ether derivatives along with the transfer of ethyl group to aldehydic carbon.
- As a reagent for copper-catalyzed asymmetric conjugate addition of alkenyl- and alkylalanes to α,β-unsaturated lactams.
- As a precursor to synthesize diethylaluminium cyanide, which is used as hydrocyanating reagent.
signalword
Danger
target_organs
Respiratory system
supp_hazards
存储类别
4.2 - Pyrophoric and self-heating hazardous materials
wgk
WGK 3
flash_point_f
-0.4 °F - closed cup
flash_point_c
-18 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Hazard Classifications
Aquatic Chronic 2 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 2 - Pyr. Liq. 1 - Repr. 2 - Self-heat. 2 - Skin Corr. 1A - STOT SE 3 - Water-react. 1
法规信息
监管及禁止进口产品
此项目有
Binuclear aluminum complexes with amine?imine type ligands derived from 1, 3-benzenedialdehyde: synthesis, structures and their catalytic properties in ring-opening polymerization.
Wu C, et al.
Journal of Coordination Chemistry, 69(6), 1066-1075 (2016)
Hydrocyanation. IV. New hydrocyanation methods using hydrogen cyanide and an alkylaluminum, and an alkylaluminum cyanide.
Nagata W, et al.
Journal of the American Chemical Society, 94(13), 4635-4643 (1972)
Copper-Catalyzed Asymmetric Conjugate Addition of Alkenyl-and Alkylalanes to ?, ?-Unsaturated Lactams.
Cottet P, et al.
Organic Letters, 15(4), 828-831 (2013)
Aliphatic Claisen rearrangement promoted by organoaluminium reagents.
Takai K, et al.
Bulletin of the Chemical Society of Japan, 57(2), 446-451 (1984)
An Alumino?Mannich Reaction of Organoaluminum Reagents, Silylated Amines, and Aldehydes.
Tarasewicz A, et al.
Chemistry?A European Journal , 24(23), 6071-6074 (2018)
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