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线性分子式:
CF3SO2OCH3
化学文摘社编号:
分子量:
164.10
UNSPSC Code:
41116105
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-371-7
Beilstein/REAXYS Number:
774772
MDL number:
产品名称
三氟甲磺酸甲酯, derivatization grade (GC derivatization), LiChropur™, 98.0%
InChI
1S/C2H3F3O3S/c1-8-9(6,7)2(3,4)5/h1H3
InChI key
OIRDBPQYVWXNSJ-UHFFFAOYSA-N
SMILES string
COS(=O)(=O)C(F)(F)F
grade
derivatization grade (GC derivatization)
assay
≥98.0% (GC)
98.0%
form
liquid
quality
LiChropur™
reaction suitability
reagent type: derivatization reagent
reaction type: Acylations
technique(s)
gas chromatography (GC): suitable
refractive index
n20/D 1.326 (lit.)
n20/D 1.327
bp
94-99 °C (lit.)
density
1.45 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Quality Level
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Application
Methyl trifluoromethanesulfonate was used in the synthesis of 2-Benzyloxy-1-methylpyridinium trifluoromethanesulfonate.
General description
Methyl trifluoromethanesulfonate (Methyl triflate) is a strong methylating agent. It is also a powerful alkylating agent and a strong irritant.
Shown to be the most effective monomethylating agent in reactions with potassium enolates.
Useful methylation reagent for the conversion of amines to methyl ammonium triflates.
Useful methylation reagent for the conversion of amines to methyl ammonium triflates.
Legal Information
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
Hazard Classifications
Acute Tox. 1 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
100.4 °F - closed cup
flash_point_c
38 °C - closed cup
法规信息
危险化学品
此项目有
W. L. F. Armarego, Christina Li Lin Chai
Purification of Laboratory Chemicals, 189-189 (2013)
Protection of Alcohols Using 2-Benzyloxy-1-Methylpyridinium Trifluoromethanesulfonate: Methyl (R)-(-)-3-Benzyloxy-2-Methyl Propanote.
Poon, Kevin WC, Philip A. Albiniak, and Gregory B. Dudley.
Organic Syntheses, 295-305 (2007)
S E Snyder et al.
Nuclear medicine and biology, 25(8), 751-754 (1998-12-24)
Synthesis of 1-[11C]methylpiperidin-4-yl propionate ([11C]PMP), an in vivo substrate for acetylcholinesterase, is reported. An improved preparation of 4-piperidinyl propionate (PHP), the immediate precursor for radiolabeling, was accomplished in three steps from 4-hydroxypiperidine by (a) protection of the amine as the
Convenient gas phase bromination of [11C]methane and production of [11C]methyl triflate.
B H Mock et al.
Nuclear medicine and biology, 26(4), 467-471 (1999-06-26)
T D Wegman et al.
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 57(4), 505-507 (2002-10-04)
This paper describes an improved preparation of [11C]verapamil by reaction of [11C]methyl triflate with desmethylverapamil. The optimal reaction temperature, amount of precursor and reaction time were assessed. With this method [11C]verapamil can be prepared with a reproducible radiochemical yield of
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