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2,3,4-Furantriol, tetrahydro-3-(phenoxymethyl)-, (3R,4R)is a furan derivative chemical compound characterized by a tetrahydrofuran ring and a phenoxymethyl group. With the molecular formula C10H16O4, 2,3,4-Furantriol, tetrahydro-3-(phenoxymethyl)-, (3R,4R)- features a specific stereochemistry, denoted by the (3R,4R)configuration, which refers to the arrangement of atoms around the chiral centers in the R configuration. Its unique structure and properties suggest potential applications in the pharmaceutical or chemical industries, warranting further research to explore its full potential.

396092-73-2

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396092-73-2 Usage

Uses

Used in Pharmaceutical Industry:
2,3,4-Furantriol, tetrahydro-3-(phenoxymethyl)-, (3R,4R)is used as a potential pharmaceutical candidate for [application reason]. Its unique structure and stereochemistry may offer advantages in the development of new drugs or therapeutic agents.
Used in Chemical Industry:
2,3,4-Furantriol, tetrahydro-3-(phenoxymethyl)-, (3R,4R)is used as a chemical intermediate or building block for [application reason]. Its specific structure and functional groups may be utilized in the synthesis of various chemical products or materials.
(Note: The specific application reasons for the pharmaceutical and chemical industries are not provided in the materials. They should be filled in based on the actual research and findings related to the compound's properties and potential uses.)

Check Digit Verification of cas no

The CAS Registry Mumber 396092-73-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,6,0,9 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 396092-73:
(8*3)+(7*9)+(6*6)+(5*0)+(4*9)+(3*2)+(2*7)+(1*3)=182
182 % 10 = 2
So 396092-73-2 is a valid CAS Registry Number.

396092-73-2Downstream Products

396092-73-2Relevant academic research and scientific papers

1-Deoxy-D-xylulose: Synthesis based on molybdate-catalyzed rearrangement of a branched-chain aldotetrose

Zhao, Shikai,Petrus, Ladislav,Serianni, Anthony S.

, p. 3819 - 3821 (2001)

equation presented 1-Deoxy-D-xylulose has been prepared in seven steps and ~21% overall yield from 2,3-O-isopropylidene-D-erythrono-1,4-lactone. The key reaction involves transformation of a branched-chain aldotetrose to the 1-deoxy-2-ketopentose catalyze

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