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N-(2,6-diisopropylphenyl)-2-methylbenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34743-31-2

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34743-31-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34743-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,7,4 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34743-31:
(7*3)+(6*4)+(5*7)+(4*4)+(3*3)+(2*3)+(1*1)=112
112 % 10 = 2
So 34743-31-2 is a valid CAS Registry Number.

34743-31-2Downstream Products

34743-31-2Relevant academic research and scientific papers

Functional Group Transposition: A Palladium-Catalyzed Metathesis of Ar-X σ-Bonds and Acid Chloride Synthesis

De La Higuera Macias, Maximiliano,Arndtsen, Bruce A.

, p. 10140 - 10144 (2018)

We describe the development of a new method to use palladium catalysis to form functionalized aromatics: via the metathesis of covalent σ-bonds between Ar-X fragments. This transformation demonstrates the dynamic nature of palladium-based oxidative addition/reductive elimination and offers a straightforward approach to incorporate reactive functional groups into aryl halides through exchange reactions. The reaction has been exploited to assemble acid chlorides without the use of high energy halogenating or toxic reagents and, instead, via the metathesis of aryl iodides with other acid chlorides.

A palladium-catalyzed carbonylation approach to acid chloride synthesis

Quesnel, Jeffrey S.,Arndtsen, Bruce A.

supporting information, p. 16841 - 16844 (2013/12/04)

We describe a new approach to acid chloride synthesis via the palladium-catalyzed carbonylation of aryl iodides. The combination of sterically encumbered phosphines (PtBu3) and CO coordination has been found to facilitate the rapid carbonylation of aryl iodides into acid chlorides via reductive elimination from (tBu3P)(CO) Pd(COAr)Cl. The formation of acid chlorides can also be exploited to perform traditional aminocarbonylation reactions under exceptionally mild conditions (ambient temperature and pressure), and with a range of weakly nucleophilic substrates.

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