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1-(4-bromo-phenacyl)-3-methyl-pyridinium; bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

136714-56-2

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136714-56-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136714-56-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,7,1 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 136714-56:
(8*1)+(7*3)+(6*6)+(5*7)+(4*1)+(3*4)+(2*5)+(1*6)=132
132 % 10 = 2
So 136714-56-2 is a valid CAS Registry Number.

136714-56-2Downstream Products

136714-56-2Relevant academic research and scientific papers

Novel one-pot three component reaction for the synthesis of [2-(alkylsulfanyl)imidazo[1,2-a]pyridin-3-yl](aryl)methanone

Kianmehr, Ebrahim,Ghanbari, Mohammad,Niri, Mehri Nadiri,Faramarzi, Reza

experimental part, p. 41 - 44 (2010/10/03)

A one-pot, three-component reaction between pyridine, phenacyl bromide, and thiocyanate is described. The reaction afforded the corresponding special type of fully substituted imidazo[1,2-a]pyridine derivatives in good yields without using any catalyst or activation.

The Mechanism of Alkylation Reactions. Part 2. The Effect of Pressure and Substituents on the Reaction of Phenacyl Bromide with Pyridine in Methanol

Forster, William,Laird, Robert M.

, p. 1033 - 1044 (2007/10/02)

Rate constants have been determined for the reaction of p-bromophenacyl bromide with pyridine and three substituents pyridines in methanol at 313.2 K.The reaction of phenacyl bromide in methanol at 313.2 K was investigated for pressures up to 100 MPa and the effect of substituents on the volume of activation, ΔV*, determined.From the partial molar volumes of reactants and products, the values of ΔV* were interpreted in terms of the intrinsic volume of the transition state, solvent electrostriction in the transition state and differences in hydrogen bonding between the initial and the transition state.The results support a transition state in which (a) bond forming leads over bond breaking and (b) considerable charge dispersal occurs.A priori calculations of ΔV and ΔV* are compared with experimental values and their utility discussed.

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