799260-82-5 Usage
Molecular structure
1,2,3,4-Butanetetrol,1-(1-methyl-1H-pyrazol-4-yl)-,(1R,2S,3R)-(9CI) has a complex molecular structure with four carbon atoms and two hydroxyl groups.
Stereochemistry
The compound has a 1R,2S,3R configuration, which determines its stereochemistry and biological activity.
Functional groups
The compound is a multi-functional alcohol, with two hydroxyl groups attached to the carbon chain.
Side chain
The compound is linked to a 1-methyl-1H-pyrazol-4-yl group, which adds to its complexity.
Uses
1,2,3,4-Butanetetrol,1-(1-methyl-1H-pyrazol-4-yl)-,(1R,2S,3R)-(9CI) is used in various industrial and pharmaceutical applications, including drug development, synthetic chemistry, and as a chemical reagent.
Importance
The compound is important due to its unique structure and properties, and has diverse applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 799260-82-5 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 799260-82:
(8*7)+(7*9)+(6*9)+(5*2)+(4*6)+(3*0)+(2*8)+(1*2)=225
225 % 10 = 5
So 799260-82-5 is a valid CAS Registry Number.
799260-82-5Relevant academic research and scientific papers
Montero, Alina,Michalik, Manfred,Feist, Holger,Reinke, Helmut,Rudloff, Ivo,Peseke, Klaus
, p. 313 - 324 (2004)
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.
