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(3R,5S)-5-(benzyloxymethyl)-3-hydroxy-dihydrofuran-2(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132454-68-3

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132454-68-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132454-68-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,4,5 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 132454-68:
(8*1)+(7*3)+(6*2)+(5*4)+(4*5)+(3*4)+(2*6)+(1*8)=113
113 % 10 = 3
So 132454-68-3 is a valid CAS Registry Number.

132454-68-3Relevant academic research and scientific papers

METHODS FOR TREATING ARENAVIRIDAE AND CORONAVIRIDAE VIRUS INFECTIONS

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Paragraph 0545, (2017/04/04)

Provided are methods for treating Arenaviridae and Coronaviridae virus infections by administering nucleosides and prodrugs thereof, of Formula I: wherein the 1′ position of the nucleoside sugar is substituted. The compounds, compositions, and methods provided are particularly useful for the treatment of Lassa virus and Junin virus infections.

METHODS AND COMPOUNDS FOR TREATING PARAMYXOVIRIDAE VIRUS INFECTIONS

-

, (2012/02/05)

Provided are methods for treating Paramyxoviridae virus infections by administering ribosides, riboside phosphates and prodrugs thereof, of Formula (I): wherein the 1 ? position of the nucleoside sugar is substituted. The compounds, compositions, and methods provided are particularly useful for the treatment of Human parainfluenza and Human respiratory syncytial virus infections

Enantioselective Synthesis of the Lactone Moiety of the Mevinic Acids using D-Xylose as a Chiral Precursor

Ballini, Roberto,Marcantoni, Enrico,Petrini, Marino

, p. 490 - 491 (2007/10/02)

Homologation of the lactone 14 easily obtained from D-xylose afforded the pyranone 15, a key chiral synthon for the lactone portion of mevinic acids.

Ring contraction of 3-deoxy-2-O-trifluoromethanesulphonates of α-hydroxy-γ-lactones to oxetanes

Witty,Fleet,Choi,Wilson,Wang,Storer,Myers,Wallis

, p. 6927 - 6930 (2007/10/02)

The ring contraction of α-triflates of 3-deoxy-1,4-lactones bearing hydrogen or alkyl substituents in the 3-position to methyl oxetane-2-carboxylates on treatment with potassium carbonate in methanol is described.

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