推荐产品
等級
for GC derivatization
品質等級
化驗
≥98.0% (GC)
98.0%
形狀
liquid
品質
LiChropur™
反應適用性
reagent type: derivatization reagent
reaction type: Acylations
技術
gas chromatography (GC): suitable
折射率
n20/D 1.326 (lit.)
n20/D 1.327
bp
94-99 °C (lit.)
密度
1.45 g/mL at 25 °C (lit.)
儲存溫度
2-8°C
SMILES 字串
COS(=O)(=O)C(F)(F)F
InChI
1S/C2H3F3O3S/c1-8-9(6,7)2(3,4)5/h1H3
InChI 密鑰
OIRDBPQYVWXNSJ-UHFFFAOYSA-N
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一般說明
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.
應用
Methyl trifluoromethanesulfonate was used in the synthesis of 2-Benzyloxy-1-methylpyridinium trifluoromethanesulfonate.
法律資訊
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany
訊號詞
Danger
危險分類
Acute Tox. 1 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
儲存類別代碼
3 - Flammable liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
100.4 °F - closed cup
閃點(°C)
38 °C - closed cup
Purification of Laboratory Chemicals, 189-189 (2013)
Protection of Alcohols Using 2-Benzyloxy-1-Methylpyridinium Trifluoromethanesulfonate: Methyl (R)-(-)-3-Benzyloxy-2-Methyl Propanote.
Organic Syntheses, 295-305 (2007)
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.
Nuclear medicine and biology, 26(4), 467-471 (1999-06-26)
Nuclear medicine and biology, 23(8), 981-986 (1996-11-01)
The important radiotracer precursor 2 beta-carbomethoxy-3 beta-(4-idophenyl)-tropane (beta-CIT, RTI-55) was made in 52% overall yield from cocaine. Key steps were improved conjugate Grignard addition to anhydroecgonine methyl ester with > 3.5:1 2 beta: 2 alpha-isomer selectivity, and a mild new
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