92001-54-2 Usage
Derivative of purine
Heterocyclic aromatic organic compound 1H-Purine, 6-chloro-8-(1-methylethyl)- is based on the purine structure, which is a heterocyclic aromatic organic compound consisting of a pyrimidine ring fused to an imidazole ring.
Chlorinated purine derivative
Presence of chloro and isopropyl (1-methylethyl) groups The structure of 1H-Purine, 6-chloro-8-(1-methylethyl)- includes a chlorine atom and an isopropyl group, making it a modified version of the purine base.
Laboratory synthesis
Not commonly found in nature 1H-Purine, 6-chloro-8-(1-methylethyl)is not a naturally occurring compound and is typically synthesized in a laboratory setting.
Medical and research purposes
Potential pharmacological properties 1H-Purine, 6-chloro-8-(1-methylethyl)- may have pharmacological properties that could be useful in the development of pharmaceutical drugs and various research applications.
Check Digit Verification of cas no
The CAS Registry Mumber 92001-54-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,0,0 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92001-54:
(7*9)+(6*2)+(5*0)+(4*0)+(3*1)+(2*5)+(1*4)=92
92 % 10 = 2
So 92001-54-2 is a valid CAS Registry Number.
92001-54-2Relevant academic research and scientific papers
DIFLUOROMETHYLATION OF UNSATURATED COMPOUNDS
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Page/Page column 53; 54, (2013/06/27)
A reagent for carrying out a difluoromethylation reaction of unsaturated compounds and ring-nitrogen-containing aromatic compounds, a zinc difluoro-methanesulfinate, as well as a method for making the reagent and a method for its use are disclosed.
Specificity of the 1-Methyladenine Receptors in Starfish Oocytes: Synthesis and Properties of Some 1,8-Disubstituted Adenines, 1,6-Dimethyl-1H-purine, and of the 1-(Azidobenzyl)adenines
Mornet, Rene,Leonard, Nelson J.,Theiler, Jane B.,Doree, Marcel
, p. 879 - 885 (2007/10/02)
A selective synthesis of 1,6-dimethylpurine (16) and the preparations of the 1-(azidobenzyl)adenines (11)-(13), 8-azido-1-benzyladenine (10), and 1-methyladenine derivatives (2)-(9) with various 8-substituents (azido, chloro, bromo, alkyl, and hydroxymeth
