1033543-75-7 Usage
Chemical structure
1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, N4-methyl-N4-(phenylmethyl)is a heterocyclic compound with a pyrazolopyrimidine core structure.
Functional groups
The compound contains two amino groups (-NH2) at the 4 and 6 positions, a methyl group (-CH3) at the N4 position, and a phenylmethyl group (-CH2-C6H5) at the N4 position.
Potential pharmaceutical applications
The compound has been studied for its potential use as a medication for various conditions due to its unique chemical structure and functional groups.
Derivative of pyrazolopyrimidine
It is a derivative of the parent compound pyrazolopyrimidine, which is known for its diverse biological activities and potential therapeutic applications.
Importance of methyl and phenylmethyl groups
The presence of a methyl group and a phenylmethyl group in the compound plays a crucial role in determining its pharmacological properties and potential therapeutic effects.
Ongoing research
Further studies are being conducted to explore the pharmaceutical properties and potential therapeutic applications of this chemical compound for certain diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 1033543-75-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,3,5,4 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1033543-75:
(9*1)+(8*0)+(7*3)+(6*3)+(5*5)+(4*4)+(3*3)+(2*7)+(1*5)=117
117 % 10 = 7
So 1033543-75-7 is a valid CAS Registry Number.
1033543-75-7Relevant academic research and scientific papers
Microwave-assisted synthesis of pyrazolo[3,4-d]pyrimidines from 2-amino-4,6-dichloropyrimidine-5-carbaldehyde under solvent-free conditions
Quiroga, Jairo,Trilleras, Jorge,Insuasty, Braulio,Abonía, Rodrigo,Nogueras, Manuel,Marchal, Antonio,Cobo, Justo
, p. 3257 - 3259 (2008/09/21)
The microwave-induced synthesis of pyrazolo[3,4-d]pyrimidines 4 in the reaction of N4-substituted-2,4-diamino-6-chloro-5-carbaldehydes 3 with hydrazine is described here. Precursors 3 have been prepared by the mono-amination of 2-amino-4,6-dich
