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Merck
CN

515884

Sigma-Aldrich

三氟甲磺酸铝

99.9% trace metals basis

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别名:
三(三氟甲烷)铝, 三(三氟甲磺酸铝)铝, 三(三氟磺酸)铝
线性分子式:
(CF3SO3)3Al
CAS号:
分子量:
474.19
MDL编号:
UNSPSC代码:
12352300
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

99.9% trace metals basis

反应适用性

core: aluminum
reagent type: catalyst

mp

300 °C (lit.)

SMILES字符串

[Al+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

1S/3CHF3O3S.Al/c3*2-1(3,4)8(5,6)7;/h3*(H,5,6,7);/q;;;+3/p-3

InChI key

FKOASGGZYSYPBI-UHFFFAOYSA-K

应用

三氟甲磺酸铝 (三氟磺酸铝或Al(OTf)3) 可用作以下反应的催化剂:
  • 通过不饱和醇的环化异构化进行环醚的区域选择性合成。
  • 糖类转化为5-羟甲基糠醛 (5-HMF)。
  • 与Pd(OAc)2/BINAP 一起参与苯乙炔的甲氧羰基化反应。

象形图

Corrosion

警示用语:

Danger

危险声明

危险分类

Eye Dam. 1 - Skin Corr. 1B

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Recyclable Pd (OAc) 2/Ligand/Al (OTf) 3 Catalyst for the Homogeneous Methoxycarbonylation and Hydrocarboxylation Reactions of Phenylacetylene
Williams DBG, et al.
Organometallics, 30(18), 4968-4973 (2011)
Aluminium (III) trifluoromethanesulfonate as an efficient catalyst for the intramolecular hydroalkoxylation of unactivated olefins: experimental and theoretical approaches
Coulombel L, et al.
Chemistry?A European Journal , 12(24), 6356-6365 (2006)
Valorization of an underused sugar derived from hemicellulose: Efficient synthesis of 5-hydroxymethylfurfural from mannose with aluminum salt catalyst in dimethyl sulfoxide/water mixed solvent
Jia S, et al.
Royal Society of Chemistry Advances, 7(62), 39221-39227 (2017)
Shaochen Zhang et al.
Science (New York, N.Y.), 364(6435), 45-51 (2019-04-06)
Accessing enantiomerically enriched amines often demands oxidation-state adjustments, protection and deprotection processes, and purification procedures that increase cost and waste, limiting applicability. When diastereomers can be formed, one isomer is attainable. Here, we show that nitriles, largely viewed as insufficiently
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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