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96227-77-9

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96227-77-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96227-77-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,2 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 96227-77:
(7*9)+(6*6)+(5*2)+(4*2)+(3*7)+(2*7)+(1*7)=159
159 % 10 = 9
So 96227-77-9 is a valid CAS Registry Number.

96227-77-9Relevant academic research and scientific papers

Synthesis of triazene-substituted homoconjugated push-pull chromophores by formal [2?+?2] cycloadditions

Erden, Kübra,Sava?, ?pek,Dengiz, Cagatay

supporting information, p. 1982 - 1985 (2019/07/03)

1-(4-Ethynylphenyl)-3,3-dialkyltriaz-1-enes, well-known building blocks for branched dendrimer syntheses, were utilized as a new type of electron-donor component in formal [2 + 2] cycloadditions. The click-type, atom-economic reactions proceed efficiently

Palladium-catalyzed carbonylative Sonogashira coupling between aryl triazenes and alkynes

Li, Wanfang,Wu, Xiao-Feng

supporting information, p. 5090 - 5093 (2015/05/13)

We developed a palladium-catalyzed carbonylative Sonogashira reaction with aryl triazenes and alkynes as substrates and methanesulfonic acid as the additive. A series of α,β-ynones were synthesized by this alternative procedure. Notably, bromides, iodides

Catalytic conversion of aryl triazenes into aryl sulfonamides using sulfur dioxide as the sulfonyl source

Li, Wanfang,Beller, Matthias,Wu, Xiao-Feng

supporting information, p. 9513 - 9516 (2014/08/18)

Various sulfonamides have been synthesized from triazenes and sulfur dioxide. In the presence of just a catalytic amount of BF3· OEt2, a series of 1-aryl-triazenes were converted into sulfonyl hydrazines in good to excellent yields. When using CuCl2 as the catalyst, the corresponding sulfonamides can be produced from the 1-aryl triazenes in good yields. This journal is the Partner Organisations 2014.

CATALYTIC RADIOFLUORINATION

-

Page/Page column 101-103, (2010/11/30)

One aspect of the present invention relates to a method of preparing radio fluorinated substituted alkyl, cycloalkyl, aryl, and alkenyl compounds. In a preferred embodiment, potassium fluoride-18 is used. Another aspect of the invention relates to arylammonium compounds containing fluorine-18 that are useful as imaging agents. In certain embodiments, the ammonium compound is a tetraaryl ammonium salt. Another aspect of the invention relates to arylsulfonium compounds containing fluorine-18 that are useful as imaging agents. In certain embodiments, the sulfonium compound is a triaryl sulfonium salt. Another aspect of the present invention relates to a method of obtaining a positron emission image of a mammal, comprising the steps of administering to a mammal a compound of the invention, and acquiring a positron emission spectrum of the mammal.

Synthesis of Biaryls from Aryltriazenes

Patrick, Timothy B.,Willaredt, Richard P.,DeGonia, David J.

, p. 2232 - 2235 (2007/10/02)

Aryltriazenes react with aromatic solvents in the presence of trifluoroacetic acid to produce biaryls.The mechanism of the reaction involves the formation of arenediazonium trifluoroacetates which lose nitrogen to give mainly aryl radicals.

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