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Benzoic acid, 2,4-bis(acetyloxy)-6-methyl-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28520-50-5

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28520-50-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28520-50-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,5,2 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 28520-50:
(7*2)+(6*8)+(5*5)+(4*2)+(3*0)+(2*5)+(1*0)=105
105 % 10 = 5
So 28520-50-5 is a valid CAS Registry Number.

28520-50-5Relevant academic research and scientific papers

Synthesis of bryophyte components 2. Syntheses of prenylated bibenzyl derivatives

Eicher,Tiefensee,Donig,Pick

, p. 98 - 102 (1991)

Efficient and expeditious syntheses of the biologically active prenylated bibenzyl derivatives 1a-d are developed giving rise to their access on a preparative scale.

Non-lithiation route to naturally occuring 5,7-dimethoxyphthalide

Kumaran, G.,Kulkarni, G. H.

, p. 436 - 437 (2007/10/02)

A non-lithiation route has been described for the synthesis of naturally occurring 5,7-dimethoxyphthalide (10) starting from ethyl orsellinate (1) involving simple reactions and less expensive reagents.

Oxidation of Alkyl 1,6-Dihydroorsellinates. A New Method for the Synthesis of Methyl Orsellinate and Homologues

Dyke, Hazel J.,Elix, John A.,Marcuccio, Sebastian M.,Whitton, Andrew A.

, p. 431 - 434 (2007/10/02)

An efficient new procedure has been developed for the oxidation of the title compounds, utilizing one mole of bromine in the presence of acetic anhydride.

Process for manufacturing alkyl-substituted β-resorcyclic acid esters

-

, (2008/06/13)

Synthetic oakmoss extracts of alkyl-substituted β-resorcylic acid esters useful as perfume ingredients, are prepared by refluxing alkyl-substituted dihydro-β-resorcylic acid esters with sulphuric acid and acetic anhydride, followed by saponifying the resultant diacetate.

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