30682-70-3 Usage
Heterocyclic organic compound
The compound consists of a ring structure containing both carbon and other non-carbon atoms (heteroatoms), such as nitrogen and sulfur.
Pyrazolopyrimidine core structure
The compound has a central structure consisting of a pyrazole ring fused to a pyrimidine ring, which contributes to its unique chemical properties.
Potential applications in pharmaceutical industry
Due to its unique chemical structure and potential biological activities, 1-methyl-1H-pyrazolo[3,4-d]pyrimidine-4,6(2H,5H)-dithione may be used as a building block in the synthesis of novel drugs.
Potential applications in agrochemical industry
The compound may be used as an active ingredient in pesticides and herbicides, providing new options for controlling pests and weeds in agriculture.
Use as a chemical probe in research and development
1-methyl-1H-pyrazolo[3,4-d]pyrimidine-4,6(2H,5H)-dithione may be utilized to study biological pathways and targets, contributing to the understanding of various biological processes.
Need for further research and exploration
To fully understand the potential uses and benefits of 1-methyl-1H-pyrazolo[3,4-d]pyrimidine-4,6(2H,5H)-dithione in various industries, more research and investigation of its properties and applications are necessary.
Check Digit Verification of cas no
The CAS Registry Mumber 30682-70-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,6,8 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 30682-70:
(7*3)+(6*0)+(5*6)+(4*8)+(3*2)+(2*7)+(1*0)=103
103 % 10 = 3
So 30682-70-3 is a valid CAS Registry Number.
30682-70-3Relevant articles and documents
Synthesis and antimicrobial activity of some heterocycles: Part-V
Bhuiyan,Rahman, Khandker M.M.,Hossain,Rahim
, p. 318 - 321 (2007/10/03)
Ortho-aminonitrile (1) was prepared from ethoxymethylenemalononitrile. 4-Allylamino-1-methyl-6-methylthiopyrazolo[3,4-d]pyrimidine (4) was prepared by an initial treatment of compound (1) with carbon disulfide in pyridine followed by methylation with methyl iodide and subsequent reaction with allylamine in acetonitrile. Orthoaminoester (5) was prepared from ethyl (ethoxymethylene) cyanoacetate. Reaction of compound (5) with formamide yielded compound (6), which was then tosylated. All compounds were screened for their antibacterial and antifungal activities.
