N,N,N-トリメチルメタンアミニウム·フルオリド(373-68-2)

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N,N,N-トリメチルメタンアミニウム·フルオリド 製品概要
化学名:N,N,N-トリメチルメタンアミニウム·フルオリド
英語化学名:Tetramethylammonium fluoride
别名:Tetramethylammonium Fluoridede;n,n,n-trimethyl-methanaminiufluoride;TETRAMETHYLAMMONIUM FLUORIDE;Tetramethylammoniumfluoride,20%AqueousSolution;Tetramethylammonium fluoride, anhydrous;Methanaminium, N,N,N-trimethyl-, fluoride;Tetramethylazanium fluoride;Tetramethylaminium·fluoride
CAS番号:373-68-2
分子式:C4H12FN
分子量:93.14
EINECS:206-769-0
カテゴリ情報:Deprotecting Reagents;Fluoride Sources;Protection and Derivatization;quarternary ammonium salts
Mol File:373-68-2.mol
N,N,N-トリメチルメタンアミニウム·フルオリド
N,N,N-トリメチルメタンアミニウム·フルオリド 物理性質
融点 170 °C (dec.) (lit.)
InChIKeyHQFTZNVQVRRDLN-UHFFFAOYSA-M
CAS データベース373-68-2(CAS DataBase Reference)
EPAの化学物質情報Tetramethylammonium fluoride (373-68-2)
安全性情報
主な危険性 Xn
Rフレーズ 20/21/22-36/37/38
Sフレーズ 26-36
RIDADR 2811
WGK Germany 3
国連危険物分類 6.1(b)
容器等級 III
HSコード 29239000
MSDS Information
ProviderLanguage
Tetramethylammonium fluoride English
N,N,N-トリメチルメタンアミニウム·フルオリド Usage And Synthesis
説明Tetramethylammonium fluoride is the quaternary ammonium salt with the formula (CH3)4NF. This hygroscopic white solid is a source of "naked fluoride", that is fluoride ions not connected to a metal atom in a complex. Most other soluble salts of fluoride are in fact bifluorides, HF2–. Historically, there has been two main approaches to prepare TMAF:
(i) Via neutralization of tetramethylammonium hydroxide (TMAOH) with HF.
(ii) through the metathesis reaction of different ammonium salts with inorganic sources of fluoride such as KF or CsF.
Due to the high basicity of the fluoride anion, the salt reacts slowly with acetonitrile, inducing its dimerization to CH3C(NH2)=CHCN, which co-crystallizes.
使用Tetramethylammonium fluoride may be used in combination with sulfuryl fluoride for the conversion of aryl phenols to aryl fluorides. It can react with aminosilanes to generate onium amide bases in situ, which can deprotonate heteroarenes.
使用Reactant for:
  • Halide-induced ring opening of 2-substituted aziridinium salts
  • Synthesis of fluoro aromatics via fluorodenitration reactions
  • Synthesis of sevoflurane in ionic liquids by halogen-exchange fluorination
  • Synthesis of fluorinated Poly(oxomolybdates)
Tags:373-68-2