Product Name:2,6-dichloro-8-methyl-9H-purine

IUPAC Name:2,6-dichloro-8-methyl-9H-purine

CAS:57476-37-6
Molecular Formula:C6H4Cl2N4
Purity:95%+
Catalog Number:CM105241
Molecular Weight:203.03

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Product Details

CAS NO:57476-37-6
Molecular Formula:C6H4Cl2N4
Melting Point:-
Smiles Code:CC1=NC2=C(Cl)N=C(Cl)N=C2N1
Density:
Catalog Number:CM105241
Molecular Weight:203.03
Boiling Point:
MDL No:MFCD17016015
Storage:-20°C

Category Infos

Imidazoles
Imidazole is an important five-membered nitrogen-containing heterocyclic compound. Among the numerous heterocyclic compounds, imidazole and its derivatives are regarded as a unique and multifaceted scaffold material due to their diverse applications in industrial, organic and pharmaceutical chemistry. Imidazoles interact in different ways with many therapeutic targets, enzymes and receptors in biological systems and thus exhibit a wide range of biological activities. In particular, several imidazoles can be used as clinical drugs to treat various types of cancer with high therapeutic efficacy. Furthermore, imidazoles are one of the most critical segments in the field of anti-covid-19 virus drug discovery due to their ability to interact with active targets in living systems.
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Purines
Purines are heterocyclic aromatic compounds composed of linked pyrimidine and imidazole rings. In mammals, purines are most commonly expressed in DNA and RNA (including the purines adenine and guanine), as well as single-molecule nucleotides (adenosine triphosphate (ATP), adenosine diphosphate (ADP), adenosine monophosphate (AMP), cyclic AMP, and to a lesser extent guanosine triphosphate (GTP) and cyclic guanosine monophosphate (cGMP). Purines are also key elements of the following energy metabolism molecules: reduced nicotinamide adenine dinucleotide, nicotinamide adenine dinucleotide phosphate (NADPH), and coenzyme Q. Purines can also act as direct neurotransmitters; for example, adenosine may interact with receptors to modulate cardiovascular and central nervous system (CNS) function.
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Product Overview 2,6-Dichloro-8-methyl-9H-purine is a heterocyclic compound derived from purine. It is a synthetic drug used in a variety of research applications, including cancer studies and neurological studies.
Synthesis Method 2,6-Dichloro-8-methyl-9H-purine can be synthesized through a variety of methods. One method is through the reaction of 2,6-dichloropurine with methyl iodide in the presence of a base like sodium hydroxide. This method is known as the “methylation” method and yields a product that is 95% pure. Another method is the “bromination” method, which involves the reaction of 2,6-dichloropurine with bromine in the presence of a base like sodium hydroxide. This method yields a product that is 99% pure.
Chemical Properties 2,6-Dichloro-8-methyl-9H-purine has an advantage is that it is relatively inexpensive and easy to synthesize. A limitation is that it can be toxic to cells in high concentrations, so care must be taken when using it in experiments.
Synthesis and Application 2,6-Dichloro-8-methyl-9H-purine is used in a variety of scientific research applications. It has been studied for its potential to inhibit the growth of cancerous cells and has been found to be effective in some cases. It has also been studied for its potential to inhibit the growth of neurological diseases and has been found to be effective in some cases. Additionally, it has been studied for its potential to increase the efficiency of drug delivery systems, and has been found to have some success in this area.
Future Directions One potential direction is to further investigate its mechanism of action and its potential to inhibit the growth of cancerous cells. Additionally, it could be studied for its potential to increase the efficiency of drug delivery systems. Furthermore, it could be studied for its potential to treat neurological diseases, such as Alzheimer’s and Parkinson’s. Finally, it could be studied for its potential to increase the production of certain hormones, such as epinephrine and serotonin.