176230
三乙基氧鎓四氟硼酸盐 溶液
1.0 M in methylene chloride
别名:
Et3OBF4, Meerwein′s reagent, Triethyloxonium fluoroborate
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关于此项目
线性分子式:
(C2H5)3O(BF4)
化学文摘社编号:
分子量:
189.99
UNSPSC Code:
12352001
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3598090
产品名称
三乙基氧鎓四氟硼酸盐 溶液, 1.0 M in methylene chloride
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
concentration
1.0 M in methylene chloride
density
1.328 g/mL at 25 °C
functional group
ether
storage temp.
2-8°C
Quality Level
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Application
用于由内酰胺制备 ω-氨基酯。
signalword
Danger
hcodes
Hazard Classifications
Carc. 2 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
target_organs
Central nervous system
supp_hazards
存储类别
6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Synthetic Communications, 18, 1625-1625 (1988)
J Aguado et al.
Biotechnology and applied biochemistry, 17 ( Pt 1), 49-55 (1993-02-01)
beta-Glucosidase from Penicillium funiculosum was immobilized on nylon powder previously activated with triethyloxonium tetrafluoroborate, 1,2-diaminoethane and glutaraldehyde. The activation of the nylon powder and the immobilization processes were studied and optimized for the enzyme and the matrix. A high activity
Some detoxification methods for N-nitrosamine-contaminated wastes.
M Castegnaro et al.
IARC scientific publications, (41)(41), 151-157 (1982-01-01)
R Ben Avraham et al.
FEBS letters, 180(2), 239-242 (1985-01-28)
Treatment of trypsin with triethyloxonium tetrafluoroborate at pH 8, 25 degrees C, results in abolition of binding to the enzyme of specific cationic substrates and inhibitors. The binding constant of soybean trypsin inhibitor to ethylated trypsin is 10000-fold smaller than
Itedale Namro Redwan et al.
The Journal of organic chemistry, 77(16), 7071-7075 (2012-07-20)
This note describes a rapid and mild strategy for the loading of alcohols and anilines onto a polystyrene triphenylmethyl (trityl) resin. High loadings were obtained in a matter of minutes by treating resin-bound trityl chloride with triethyloxonium tetrafluoroborate followed by
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