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线性分子式:
LiAlH[OC(CH3)3]3
化学文摘社编号:
分子量:
254.27
UNSPSC Code:
12352000
NACRES:
NA.22
PubChem Substance ID:
EC Number:
241-490-8
Beilstein/REAXYS Number:
5796791
MDL number:
Assay:
97%
产品名称
三叔丁氧基氢化铝锂, 97%
InChI
1S/3C4H9O.Al.Li.H/c3*1-4(2,3)5;;;/h3*1-3H3;;;/q3*-1;+2;+1;
InChI key
BYBIDFZFKATBFH-UHFFFAOYSA-N
SMILES string
[H][Al]([Li])(OC(C)(C)C)(OC(C)(C)C)OC(C)(C)C
assay
97%
reaction suitability
reagent type: reductant
mp
300-319 °C (dec.) (lit.)
Quality Level
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Application
- 还原剂
三- 叔 -丁氧基氢化铝 (LTBA) 锂是一种稳定 的温和还原剂,用于在酯存在下选择性还原醛和酮。它也可用于将亚氨酰氯还原为醛亚胺 以及将芳香族二硫化物还原为相应的的硫醇。
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B - Water-react 1
supp_hazards
存储类别
4.3 - Hazardous materials which set free flammable gases upon contact with water
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Facile preparation of polyfluoroalkylated aldimines from polyfluoroalkanoic acids.
Takagi J, et al.
Synthesis, 2007(11), 1624-1628 (2007)
Electrolytic Decarboxylation. 6. A Convenient Synthesis of 3-(cis-3-Hexenyl)-2-cyclopentenone, a Precursor of cis-Jasmone Synthesis.
Torii S, et al.
Bulletin of the Chemical Society of Japan, 55(12), 3947-3948 (1982)
Remarkably facile reductive opening of tetrahydrofuran and related ethers by lithium tri-tert-butoxyaluminohydride in the presence of triethylborane.
Brown H C, et al.
Journal of the American Chemical Society, 94(5), 1750-1751 (1972)
Rapid and selective reduction of functionalized aromatic disulfides with lithium tri-tert-butoxyaluminohydride. A remarkable steric and electronic control. Comparison of various hydride reagents.
Krishnamurthy S and Aimino D
The Journal of Organic Chemistry, 54(18), 4458-4462 (1989)
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