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dimethyl 4-hydroxy-4H-chromene-2,3-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56529-99-8

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56529-99-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56529-99-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,5,2 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56529-99:
(7*5)+(6*6)+(5*5)+(4*2)+(3*9)+(2*9)+(1*9)=158
158 % 10 = 8
So 56529-99-8 is a valid CAS Registry Number.

56529-99-8Downstream Products

56529-99-8Relevant academic research and scientific papers

Metal-free catalytic cascade to chromones: Direct coupling of salicylaldehydes and activated alkynes triggered by aryloxyl radicals

Wang, Ping,Li, Zhongfeng,Cao, Shengli,Rao, Honghua

, p. 106350 - 106354 (2016/01/09)

The first intermolecular addition reaction of aryloxyl radicals to CC bonds was disclosed, which can afford biologically important chromone scaffolds via a PhNMe3I-catalyzed direct coupling of readily available salicylaldehydes and activated internal alkynes in only one step, and can tolerate a range of catalytically reactive functional groups.

A green and rapid approach for the stereoselective vinylation of phenol, thiol and amine derivatives in water

Sarrafi, Yaghoub,Sadatshahabi, Marzieh,Alimohammadi, Kamal,Tajbakhsh, Mahmood

supporting information; experimental part, p. 2851 - 2858 (2011/11/06)

The stereoselective formation of C-O, C-S and C-N bonds by the reaction of phenols, thiols and amines with activated alkynes is described. The reactions are successfully conducted in water with excellent yields at room temperature. The lack of organic sol

Reaction between ortho-hydroxy aromatic aldehydes and dialkyl acetylenedicarboxylates in the presence of silica gel in solvent-free conditions

Noshiranzadeh, Nader,Ramazani, Ali

, p. 3181 - 3189 (2008/02/12)

A two-component condensation reaction between an ortho-hydroxy aromatic aldehyde and an electron-poor acetylenic ester efficiently provides fully substituted electron-poor aryl vinyl ethers and chromenes in a one-pot reaction in the presence of silica-gel in solvent-free conditions. Copyright Taylor & Francis Group, LLC.

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