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Merck
CN

281077

三甲基氧鎓四氟硼酸盐

95%

别名:

三甲基氧鎓氟硼酸盐

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关于此项目

线性分子式:
(CH3)3O(BF4)
化学文摘社编号:
分子量:
147.91
UNSPSC Code:
12352107
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-994-4
Beilstein/REAXYS Number:
3597303
MDL number:
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产品名称

三甲基氧鎓四氟硼酸盐, 95%

InChI key

CZVZBKHWOFJNCR-UHFFFAOYSA-N

InChI

1S/C3H9O.BF4/c1-4(2)3;2-1(3,4)5/h1-3H3;/q+1;-1

SMILES string

C[O+](C)C.F[B-](F)(F)F

assay

95%

form

solid

functional group

ether

storage temp.

−20°C

Quality Level

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Application

进行羟基甲基化,最近用于复杂、多步定向合成海洋天然产物 spirastrellolide。

General description

三甲基氧鎓四氟硼酸盐可用作羟基/羧基官能团甲基化反应的甲基化试剂。它能够使多功能羧酸甲基化。它还可用作环状硫化物和醚聚合的催化剂。

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Toward the total synthesis of spirastrellolide A. Part 2: Conquest of the northern hemisphere.
Alois Fürstner et al.
Angewandte Chemie (International ed. in English), 45(33), 5510-5515 (2006-08-15)
H M Liebich et al.
Journal of chromatography. B, Biomedical sciences and applications, 713(2), 427-432 (1998-09-24)
We developed a new sample preparation method for profiling organic acids in urine by GC or GC-MS. The method includes derivatisation of the organic acids directly in the aqueous urine using trimethyloxonium tetrafluoroborate as a methylating agent, extraction of the
Marco Pacenti et al.
Biomedical chromatography : BMC, 22(10), 1155-1163 (2008-05-29)
A method for the determination of the organic acids directly in the urine employing derivatization with trimethyloxonium tetrafluoroborate as a methylating agent and sequential extraction by head space and direct immersion/solid phase microextraction is reported. Furoic acid, hippuric acid, methylhippuric
S Chericoni et al.
Journal of analytical toxicology, 35(4), 193-198 (2011-04-26)
The present work describes the validation of a novel aqueous in situ derivatization procedure with trimethyloxonium tetrafluoroborate (TMO) as methylating agent for the simultaneous, quantitative analysis of Δ(9)-tetrahydrocannabinol (THC) and 11-nor-Δ(9)-tetrahydrocannabinol carboxylic acid (THC-COOH) in human urine. The derivatizing agent
H M Liebich et al.
Journal of chromatography. A, 843(1-2), 237-245 (1999-07-10)
Trimethyloxonium tetrafluoroborate (TMO) is applied as derivatising reagent to transform urinary organic acids into their methyl esters. The method is suggested as an alternative to the use of diazomethane which is carcinogenic and explosive. In contrast to other methods avoiding

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