产品名称
三乙基氧鎓四氟硼酸盐, ≥97.0% (T)
InChI
1S/C6H15O.BF4/c1-4-7(5-2)6-3;2-1(3,4)5/h4-6H2,1-3H3;/q+1;-1
SMILES string
F[B-](F)(F)F.CC[O+](CC)CC
InChI key
IYDQMLLDOVRSJJ-UHFFFAOYSA-N
assay
≥97.0% (T)
form
crystals
contains
1-3% ether as stabilizer
solubility
methylene chloride: 20 mg/mL, clear, colorless
functional group
ether
storage temp.
2-8°C
Quality Level
Application
三乙基氧四氟硼酸盐可用于:
- 与内酰胺反应,水解制备氨基酯。
- 通过[3 + 2]-环加成反应,由氮丙啶和腈制备取代的咪唑啉。
- 一系列 N-芳基磺酰基-α-氨基酸甲基酯的 N-烷基化,这些甲基酯在磺酰胺芳环第4位有可变取代基。
Other Notes
强效乙基化剂;用于酸的酯化反应;以及蛋白质羧基残基的改性
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
supp_hazards
存储类别
8A - Combustible, corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
监管及禁止进口产品
此项目有
N-Alkylation of N-arylsulfonyl-α-amino acid methyl esters by trialkyloxonium tetrafluoroborates
De Marco R, et al.
Tetrahedron, 67(50), 9708-9714 (2011)
Synthesis of substituted imidazolines via [3+ 2]-cycloaddition of aziridines with nitriles
Prasad BAB, et al.
Tetrahedron Letters, 45(6), 1137-1141 (2004)
H. Meerwein et al.
Angewandte Chemie (International Edition in English), 72, 927-927 (1960)
A mild and facile route to ω-amino esters
Menezes, R and Smith, MB
Synthetic Communications, 18(14), 1625-1636 (1988)
The nature of amino acid side chains which are critical for the activity of lysozyme.
S M Parsons et al.
Biochemistry, 8(2), 700-712 (1969-02-01)
我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持