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Benzoic acid, 2-[[(trifluoromethyl)sulfonyl]oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

171016-63-0

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171016-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 171016-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,0,1 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 171016-63:
(8*1)+(7*7)+(6*1)+(5*0)+(4*1)+(3*6)+(2*6)+(1*3)=100
100 % 10 = 0
So 171016-63-0 is a valid CAS Registry Number.

171016-63-0Relevant academic research and scientific papers

Carboxylate-Assisted Oxidative Addition to Aminoalkyl PdII Complexes: C(sp3)?H Arylation of Alkylamines by Distinct PdII/PdIV Pathway

Whitehurst, William G.,Blackwell, J. Henry,Hermann, Gary N.,Gaunt, Matthew J.

supporting information, p. 9054 - 9059 (2019/06/04)

Reported is the discovery of an approach to functionalize secondary alkylamines using 2-halobenzoic acids as aryl-transfer reagents. These reagents promote an unusually mild carboxylate-assisted oxidative addition to alkylamine-derived palladacycles. In the presence of AgI salts, a decarboxylative C(sp3)?C(sp2) bond reductive elimination leads to γ-aryl secondary alkylamines and renders the carboxylate motif a traceless directing group. Stoichiometric mechanistic studies were effectively translated to a Pd-catalyzed γ-C(sp3)?H arylation process for secondary alkylamines.

A concise synthesis of arnottin I via internal biaryl coupling reaction using palladium reagent

Harayama, Takashi,Yasuda, Hirotake

, p. 61 - 64 (2007/10/03)

Total synthesis of arnottin I (1) was accomplished via the internal arylaryl coupling reaction of iodo-ester (2) by the palladium-assisted cyclization reaction.

A Direct Route to the Pyrrolobenzodiazepine Ring System Using Aryl Triflates

Kraus, George A.,Liu, Peng

, p. 7595 - 7598 (2007/10/02)

The pyrrolobenzodiazepine and dibenzodiazepine skeletons were rapidly generated from salicylic acids.The key step in these syntheses was the substitution of an aryl triflate.

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