799260-83-6 Usage
Isomer of erythritol
Erythritol is a sugar alcohol found in some fruits and fermented foods. The compound is an isomer, meaning it has the same molecular formula but a different arrangement of atoms.
Tetrahydroxy derivative of butane
The compound is derived from butane, a four-carbon alkane, with four hydroxyl (OH) groups attached to the carbon atoms.
Contains a pyrazole group
Pyrazole is a biologically active heterocyclic compound, which may contribute to the compound's potential biological activity.
(1R,2R,3R) configuration
This indicates the stereochemistry of the compound, specifically the arrangement of the hydroxyl groups on the carbon atoms.
Potential applications in the pharmaceutical industry
Due to its unique structure and potential biological activity, the compound may have uses in the development of new drugs or therapies.
Further research needed
To fully understand the properties and potential uses of the compound, additional research is required.
Check Digit Verification of cas no
The CAS Registry Mumber 799260-83-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,9,2,6 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 799260-83:
(8*7)+(7*9)+(6*9)+(5*2)+(4*6)+(3*0)+(2*8)+(1*3)=226
226 % 10 = 6
So 799260-83-6 is a valid CAS Registry Number.
799260-83-6Relevant academic research and scientific papers
Synthesis of substituted 1-\C\-phenyl-D-tetritols and 1-C-(1H-pyrazol-4-yl) -D-tetritols by ring transformation of 2-formylglycals
Montero, Alina,Michalik, Manfred,Feist, Holger,Reinke, Helmut,Rudloff, Ivo,Peseke, Klaus
, p. 313 - 324 (2007/10/03)
2-Formylglycals 1a,b reacted with dialkyl 3-oxoglutarates in the presence of base to furnish the 5-[(1R,2R(S),3R)-1,2,4-tris(benzyloxy)-3-hydroxy-butyl]- 2-hydroxy-isophthalic acid dialkyl esters 2a-d. Treatment of 1a,b with hydrazine derivatives afforded the substituted 1,2,4-tri-O-benzyl-1C-(1H-pyrazol-4-yl)-D- tetritols 5a-d. Deprotection of 5a,b was achieved with Pd/H2 to yield the 1C-(1-methyl-1H-pyrazol-4-yl)-D-tetritols 6a,b. Copyright by Marcel Dekker, Inc.
