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acetoxy(p-methoxyphenoxy) methane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57440-09-2

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57440-09-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57440-09-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,4,4 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 57440-09:
(7*5)+(6*7)+(5*4)+(4*4)+(3*0)+(2*0)+(1*9)=122
122 % 10 = 2
So 57440-09-2 is a valid CAS Registry Number.

57440-09-2Downstream Products

57440-09-2Relevant academic research and scientific papers

THE SYNTHESIS, CHARACTERISATION AND REACTIVITY OF SOME LEAD(IV) CARBOXYLATES

Buston, Jonathan E. H.,Coop, Andrew,Keady, Richard,Moloney, Mark G.,Thompson, Russell M.

, p. 1101 - 1116 (2007/10/02)

A detailed examination of the preparation, characterisation and reactivity of a range of lead(IV) carboxylates is reported.The replacement of the acetate ligands of lead(IV) tetraacetate by other carboxylates gives the lead(IV) tetracarboxylates 1-16, which have usually been found to be more stable than lead tetraacetate with respect to hydrolysis.These compounds react with allyltributylstannane to give high yields of the corresponding allyl esters 20-34 under mild conditions.

Syntheses of Sulfinylmethyl Ethers and Conversion of these into Halomethyl and Acyloxymethyl Ethers

Antonsen, Oeyvind,Benneche, Tore,Undheim, Kjell

, p. 515 - 523 (2007/10/02)

Halomethyl ethers can be prepared from sulfinyl ethers by cleavage of the carbon-sulfur bond with thionyl chloride, acetyl chloride or trimethylsilyl halides.In the presence of alkenyl groups in the substrate, acetyl chloride is the reagent of choice.Trifluoroacetic anhydride reacts in the same manner to form the trifluoroacetoxymethyl ether.With acetic anhydride, catalysis by methanesulfonic acid was required.At elevated temperatures in the presence of sodium acetate the products were formed by the Pummerer rearrangement.

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