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About This Item
线性分子式:
Bi(OSO2CF3)3
CAS号:
分子量:
656.19
MDL號碼:
分類程式碼代碼:
12161600
PubChem物質ID:
NACRES:
NA.22
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反應適用性
core: bismuth
reagent type: catalyst
mp
>300 °C (lit.)
SMILES 字串
[Bi+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.Bi/c3*2-1(3,4)8(5,6)7;/h3*(H,5,6,7);/q;;;+3/p-3
InChI 密鑰
NYENCOMLZDQKNH-UHFFFAOYSA-K
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應用
三氟甲磺酸铋 (Ⅲ) 可在下列过程中用作催化剂：
- 缩醛脱保护
- 噻吩和呋喃的 2- 叔 丁氧基衍生物的裂解
- 缩醛烯丙基化形成高烯丙基醚
催化烯丙基、炔丙基和苄基醇与磺胺类、氨基甲酸酯类和甲酰胺类的直接取代。
包裝
三氟甲磺酸铋 (Ⅲ) 是一种环保的路易斯酸，可通过三氟乙酸与三氟乙酸铋 (Ⅲ) 反应制备。
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
其他客户在看
Bismuth (III) trifluoromethanesulfonate: An efficient catalyst for the sulfonylation of arenes.
Repichet S, et al.
The Journal of Organic Chemistry, 64, 6479-6482 (1999)
Bismuth (III) triflate in organic synthesis.
Gaspard-Iloughmane H and Le Roux C.
European Journal of Organic Chemistry, 2004(12), 2517-2532 (2004)
Maria Ricciardi et al.
ChemSusChem, 10(10), 2291-2300 (2017-04-05)
The disposal of any waste by recovering it within the production plant represents the ultimate goal of every biorefinery. In this scenario, the selective preparation of monoalkyl glyceryl ethers (MAGEs) starting from glycidol, obtained as byproduct in the epichlorohydrin production
Applications of bismuth (III) compounds in organic synthesis.
Leonard NM, et al.
Tetrahedron, 58(42), 8373-8397 (2002)
Raffaele Cucciniello et al.
ChemSusChem, 9(23), 3272-3275 (2016-11-24)
The present work deals with the production of monoalkyl glyceryl ethers (MAGEs) through a new reaction pathway based on the reaction of glycidol and alcohols catalyzed by Lewis acid-based catalysts. Glycidol is quantitatively converted with high selectivity (99 %) into MAGEs
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