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α,α,α-Trifluoro-2,4,6-trinitrotoluene, also known as TF-TNT, is a chemical compound that is a derivative of trinitrotoluene (TNT). It is characterized by the presence of three fluorine atoms attached to the alpha carbon atoms of the methyl groups in the TNT molecule, which significantly alters its properties compared to the parent compound. TF-TNT exhibits enhanced thermal stability and reduced sensitivity to shock, making it a potential candidate for applications in the field of explosives. The introduction of fluorine atoms also results in a higher density and increased energy content, which can be advantageous in certain explosive formulations. However, the synthesis and handling of TF-TNT require careful consideration due to its potential reactivity and the need to manage the risks associated with handling energetic materials.

651-94-5

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651-94-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 651-94-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,5 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 651-94:
(5*6)+(4*5)+(3*1)+(2*9)+(1*4)=75
75 % 10 = 5
So 651-94-5 is a valid CAS Registry Number.

651-94-5Downstream Products

651-94-5Relevant academic research and scientific papers

Trifluoromethylation of 1,3,5-Trinitrobenzene

Stahly, G. Patrick

, p. 431 - 434 (1989)

The trifluoromethyl anion was trapped as Meisenheimer complex 2 on heating a mixture of potassium trifluoroacetate and 1,3,5-trinitrobenzene (TNB) in DMF or DMSO.Treatment of 2 with tert-butylhypochlorite afforded 1-trifluoromethyl-2,4,6-trinitrobenzene (

Stable gem-trifluoromethyl anionic σ-complexes based on 1,3,5-tris(sulfonyl)benzene derivatives and their transformations

Holovko-Kamoshenkova, Oksana M.,Kirij, Nataliia V.,Boiko, Vladimir N.,Rozhenko, Alexander B.,Yagupolskii, Yurii L.

experimental part, p. 1344 - 1352 (2011/02/22)

A convenient synthetic procedures is described to obtain gem-trifluoromethyl anionic σ-complexes of 1,3,5-tris(fluorosulfonyl) benzene, 1,3,5-tris(β,β,β-trifluoroethoxysulfonyl)benzene, 1,3,5-tris(trifluoromethylsulfonyl)benzene as well as of 1,3,5-trinot

Oxidative nucleophilic substitution of hydrogen in nitroarenes with trifluoromethyl carbanions. Synthesis of trifluoromethyl phenols

Surowiec, Marek,Ma?kosza, Mieczys?aw

, p. 5019 - 5024 (2007/10/03)

Trifluoromethyl carbanions generated from the Ruppert reagent and TASF add to highly electron-deficient nitroarenes to produce σH adducts subsequently oxidized with dimethyldioxirane to substituted trifluoromethyl phenols.

Synthesis of trifluoromethyl aryl derivatives via difluorocarbene precursors and nitro-substituted aryl chlorides

Duan, Jian-Xing,Su, De-Bao,Wu, Jian-Ping,Chen, Qing-Yun

, p. 167 - 170 (2007/10/02)

Treatment of aryl chlorides containing electron-withdrawing proups with methyl fluorosulfonyl difluoroacetate or methyl halodifluoroacetate in the presence of potassium fluoride and copper iodide gave the corresponding trifluoromethyl derivatives in moderate to high yields.

Perfluoroalkylation process

-

, (2008/06/13)

Despite the instabity of perfluoralkyl anions, it is possible to perfluoroalkylate aromatic compounds if appropriately substituted by suitable electronegative substituents (e.g., nitro, trifluoromethylsulfonyl, etc.). Thus a novel Meisenheimer complex is

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