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diethyl 3-bromo-2-phenylpropene-1,1-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106352-17-4

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106352-17-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106352-17-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,3,5 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 106352-17:
(8*1)+(7*0)+(6*6)+(5*3)+(4*5)+(3*2)+(2*1)+(1*7)=94
94 % 10 = 4
So 106352-17-4 is a valid CAS Registry Number.

106352-17-4Relevant academic research and scientific papers

Zinc-mediated addition of diethyl bromomalonate to alkynes for the cascade reaction towards polysubstituted pyranones and tetracarbonyl derivatives

Miersch, Anne,Harms, Klaus,Hilt, Gerhard

supporting information, p. 542 - 544 (2014/01/06)

The zinc-mediated regioselective addition reactions of diethyl bromomalonate and aromatic and aliphatic alkynes were investigated for the synthesis of vinyl malonates. When the vinyl organo-zinc intermediates were reacted with acid chlorides 2H-pyran-2-ones were obtained while the application of oxalyl chloride and an amine led to tetracarbonyl derivatives in a one-pot multi-step reaction sequence. The Royal Society of Chemistry 2014.

New routes to polyfunctionally substituted benzene, pyridazines and thiophene derivatives

Erian, Ayman Wahba,Abdel, Abu Zeid,Hassanien, Baset,Mohamed, Nadia Ragab

, p. 147 - 155 (2007/10/03)

Diethyl 2-phenyl-3-thiocyanopropene-1,1-dicarboxylate (3) as a key precursor in heterocyclic synthesis. The applicability and synthetic potency of 3 are studied to afford unique heterocyclic compounds.

Diethyl 2-aryl-3-cyanopropene-1,1-dicarboxylates: New versatile precursors in heterocyclic synthesis

Erian, Ayman W.,Araki, Vivian F.,Aziz, Suzan I.,Sherif, Sherif M.

, p. 661 - 669 (2007/10/03)

An expeditious synthetic route for the title precursor is reported. It provides access to a variety of polyfunctionally substituted pyridines, pyridazines, pyrazolopyridines, thiophenes, and thienopyridines.

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