188949-71-5 Usage
Chemical structure
A cyclohexene carboxylic acid derivative with an ethyl ester group and a purine moiety attached to the carboxylic acid.
Potential applications
Pharmaceutical applications, drug development, and medicinal chemistry.
Enzyme-catalyzed conversion
Acts as a potential substrate for enzyme-catalyzed conversion to active metabolites.
Immune system effects
May have inhibitory effects on the immune system.
Synthesis of pharmacologically active compounds
Serves as a precursor for the synthesis of pharmacologically active compounds.
Molecular weight
Approximately 343.78 g/mol
Functional groups
Carboxylic acid, ester, and purine.
Solubility
Likely soluble in organic solvents such as ethanol, methanol, or dimethyl sulfoxide (DMSO).
Stability
May be sensitive to hydrolysis, oxidation, and other chemical reactions, depending on the reaction conditions and presence of catalysts or reagents.
Check Digit Verification of cas no
The CAS Registry Mumber 188949-71-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,9,4 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 188949-71:
(8*1)+(7*8)+(6*8)+(5*9)+(4*4)+(3*9)+(2*7)+(1*1)=215
215 % 10 = 5
So 188949-71-5 is a valid CAS Registry Number.
188949-71-5Relevant academic research and scientific papers
Synthesis and conformational study of 3-hydroxy-4-(hydroxymethyl)-1-cyclohexanyl purines and pyrimidines
Maurinsh, Yuris,Schraml, Jan,De Winter, Hans,Blaton, Norbert,Peeters, Oswald,Lescrinier, Eveline,Rozenski, Jef,Van Aerschot, Arthur,De Clercq, Erik,Busson, Roger,Herdewijn, Piet
, p. 2861 - 2871 (2007/10/03)
The cyclohexane nucleosides with a 1,4-relationship between nucleoside base and hydroxymethyl moiety were synthesized using a conjugated addition reaction of the nucleobases to ethyl 1,3-cyclohexadiene-1-carboxylate and hydroboration of the cyclohexenyl precursor. The lack of antiviral activity of the compounds was correlated with the conformation of these nucleosides as deduced from NMR and X-ray analysis.
