430609
三氟甲磺酸镧(III)
99.999% trace metals basis
别名:
La(OTf)3, 三氟甲磺酸镧, 三（三氟甲烷）镧, 三氟甲基磺酸镧(III), 三氟甲磺酸 镧盐
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关于此项目
线性分子式:
(CF3SO3)3La
化学文摘社编号:
分子量:
586.11
UNSPSC Code:
12161600
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
9009103
InChI
1S/3CHF3O3S.La/c3*2-1(3,4)8(5,6)7;/h3*(H,5,6,7);/q;;;+3/p-3
SMILES string
[La+3].[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F
InChI key
WGJJZRVGLPOKQT-UHFFFAOYSA-K
assay
99.999% trace metals basis
reaction suitability
core: lanthanum, reagent type: catalyst
Quality Level
Application
一种耐水路易斯酸，用于硅烯醇醚与醛的羟醛反应。
存储类别
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Jie Wu et al.
Bioresource technology, 324, 124664-124664 (2021-01-18)
Previous work has shown that sulfonation and oxidation of chemi-thermomechanical pulps (CTMPs) significantly enhanced enzyme accessibility to cellulose while recovering the majority of carbohydrates in the water-insoluble component. In the work reported here, modified (sulfonated and oxidized) CTMPs derived from
The Journal of Organic Chemistry, 59, 3590-3590 (1994)
Sandro Keller et al.
Analytical chemistry, 84(11), 5066-5073 (2012-04-26)
Isothermal titration calorimetry (ITC) is a powerful classical method that enables researchers in many fields to study the thermodynamics of molecular interactions. Primary ITC data comprise the temporal evolution of differential power reporting the heat of reaction during a series
Yan-ping Zhu et al.
Organic letters, 14(20), 5378-5381 (2012-10-13)
An I(2)-CF(3)SO(3)H synergistic promoted sp(3) C-H bond diarylation protocol was developed for the synthesis of 2,2-bis(4-(dimethylamino)phenyl)-1-aryl ethanones. The reaction performed well in the absence of any metal and ligand. It integrated three reactions with different mechanisms (iodination, Kornblum oxidation, and
Yusuke Imazaki et al.
Journal of the American Chemical Society, 134(36), 14760-14763 (2012-08-25)
Aryl triflates were transformed to aryl bromides/iodides simply by treating them with LiBr/NaI and [Cp*Ru(MeCN)(3)]OTf. The ruthenium complex also catalyzed the transformation of alkenyl sulfonates and phosphates to alkenyl halides under mild conditions. Aryl and alkenyl triflates undergo oxidative addition
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