396092-72-1 Usage
Uses
Used in Organic Synthesis:
2,3,4-Furantriol, tetrahydro-3-(hydroxymethyl)-, (3R,4R)(9CI) is used as a reagent in organic synthesis for its ability to facilitate the formation of complex organic molecules. Its multiple hydroxyl and hydroxymethyl groups make it a versatile component in the creation of various chemical compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2,3,4-Furantriol, tetrahydro-3-(hydroxymethyl)-, (3R,4R)(9CI) is used as a building block for the development of new drugs. Its unique structure allows it to be incorporated into the design of pharmaceuticals, potentially enhancing their efficacy and selectivity.
Used in Chemical Production:
2,3,4-Furantriol, tetrahydro-3-(hydroxymethyl)-, (3R,4R)(9CI) is also utilized in the production of other chemicals, where its functional groups can be exploited to create a wide range of chemical products with diverse applications.
Used in Research and Development:
Due to its potential biological activity, 2,3,4-Furantriol, tetrahydro-3-(hydroxymethyl)-, (3R,4R)(9CI) is used in research and development for exploring its pharmaceutical applications. Scientists are interested in its unique structural properties and how they might contribute to the development of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 396092-72-1 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 396092-72:
(8*3)+(7*9)+(6*6)+(5*0)+(4*9)+(3*2)+(2*7)+(1*2)=181
181 % 10 = 1
So 396092-72-1 is a valid CAS Registry Number.
396092-72-1Relevant academic research and scientific papers
Hricoviniova, Zuzana,Hricovini, Milos,Petrus, Ladislav
, p. 827 - 836 (2000)
2-C-(Hydroxymethyl)-D-erythrose (2) and 2-C-(hydroxymethyl)-D-threose (4) have been stereospecifically synthesized in one-step by a molybdic acid-catalysed isomerization reaction from respective D-xylulose (1) and D-ribulose (3). In the case of interconversion of 1 to 2, the content of the 2-C-branched chain tetrose in the equilibrium mixture can be doubled if boric acid is present in the reaction mixture in addition to the catalyst.
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 (2007/10/03)
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
