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4-fluoro-N-(2-methylprop-2-en-1-yl)aniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

225642-31-9

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225642-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 225642-31-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,5,6,4 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 225642-31:
(8*2)+(7*2)+(6*5)+(5*6)+(4*4)+(3*2)+(2*3)+(1*1)=119
119 % 10 = 9
So 225642-31-9 is a valid CAS Registry Number.

225642-31-9Relevant academic research and scientific papers

Cp2TiX Complexes for Sustainable Catalysis in Single-Electron Steps

Richrath, Ruben B.,Olyschl?ger, Theresa,Hildebrandt, Sven,Enny, Daniel G.,Fianu, Godfred D.,Flowers, Robert A.,Gans?uer, Andreas

, p. 6371 - 6379 (2018)

We present a combined electrochemical, kinetic, and synthetic study with a novel and easily accessible class of titanocene catalysts for catalysis in single-electron steps. The tailoring of the electronic properties of our Cp2TiX-catalysts that

Mechanism-Based Condition Screening for Sustainable Catalysis in Single-Electron Steps by Cyclic Voltammetry

Liedtke, Theresa,Spannring, Peter,Riccardi, Ludovico,Gans?uer, Andreas

supporting information, p. 5006 - 5010 (2018/03/30)

A cyclic-voltammetry-based screening method for Cp2TiX-catalyzed reactions is introduced. Our mechanism-based approach enables the study of the influence of various additives on the electrochemically generated active catalyst Cp2TiX, which is in equilibrium with catalytically inactive [Cp2TiX2]?. Thioureas and ureas are most efficient in the generation of Cp2TiX in THF. Knowing the precise position of the equilibrium between Cp2TiX and [Cp2TiX2]? allowed us to identify reaction conditions for the bulk electrolysis of Cp2TiX2 complexes and for Cp2TiX-catayzed radical arylations without having to carry out the reactions. Our time- and resource-efficient approach is of general interest for the design of catalytic reactions that proceed in single-electron steps.

Palladium-catalyzed cyclization/cyclopropanation reaction for the synthesis of fused N-containing heterocycles

Nandi, Sukla,Ray, Jayanta K.

scheme or table, p. 6993 - 6997 (2010/02/27)

Palladium-catalyzed cyclization/cyclopropanation can be used to convert a range of substituted cyclic N-aryl allyl/methallyl amines efficiently and selectively to the corresponding fused tetrahydropyridine/cyclopropane-fused isoquinoline derivatives via β

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