CAS 3035-73-2
:9H-Purin-2-amine, 6-chloro-9-methyl-
Description:
9H-Purin-2-amine, 6-chloro-9-methyl-, also known as 6-chloro-9-methyladenine, is a purine derivative characterized by its structural features that include a purine base with a methyl group at the 9-position and a chlorine atom at the 6-position. This compound is typically a white to off-white solid and is soluble in polar solvents such as water and alcohols. It exhibits properties typical of purines, including the ability to participate in hydrogen bonding due to the presence of amino and nitrogen atoms in its structure. As a derivative of adenine, it may play a role in biological systems, particularly in nucleic acid metabolism and signaling pathways. The compound is of interest in various fields, including biochemistry and pharmacology, due to its potential applications in research and therapeutic contexts. Its CAS number, 3035-73-2, allows for easy identification and reference in scientific literature and databases.
Formula:C6H6ClN5
Synonyms:- 6-Chloro-9-methyl-9H-purin-2-amine
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Found 4 products.
6-Chloro-9-methyl-9H-purin-2-amine
CAS:6-Chloro-9-methyl-9H-purin-2-aminePurity:95%Molecular weight:183.6g/mol6-chloro-9-methyl-9H-purin-2-amine
CAS:Formula:C6H6ClN5Purity:95%Color and Shape:SolidMolecular weight:183.66-chloro-9-methyl-9H-purin-2-amine
CAS:6-chloro-9-methyl-9H-purin-2-amine is a cytostatic agent that is used in the synthesis of other compounds. It is prepared by the quaternization of 6-chloropurine with methylmagnesium chloride followed by amination with methyl iodide. Purinium chloride is then obtained by reacting chloroform with potassium hydrogen fluoride and hydrochloric acid. This product can be used as an intermediate in the synthesis of purines, x-rays, and iodides. 6-Chloro-9-[methyl(3,5,6 -trimethylphenyl)amino]purin-2 amine has been shown to have cytostatic activity against human lymphocytes in vitro.
Formula:C6H6ClN5Purity:Min. 95%Molecular weight:183.6 g/mol
