CAS 1681-19-2: 2-chloro-6-methyl-5H-purine

Description: 2-Chloro-6-methyl-5H-purine, with the CAS number 1681-19-2, is a purine derivative characterized by its bicyclic structure, which consists of a fused imidazole and pyrimidine ring. This compound features a chlorine atom at the 2-position and a methyl group at the 6-position of the purine ring, influencing its chemical reactivity and biological activity. It is typically a crystalline solid, exhibiting moderate solubility in polar solvents. The presence of the chlorine substituent can enhance its reactivity, making it of interest in various chemical syntheses and biological applications. 2-Chloro-6-methyl-5H-purine may also exhibit pharmacological properties, potentially acting as a nucleobase analog or influencing nucleic acid metabolism. Its structural characteristics allow it to participate in various chemical reactions, including substitution and addition reactions, which are essential in medicinal chemistry and drug development. Overall, this compound serves as a valuable building block in the synthesis of more complex molecules in both research and pharmaceutical contexts.

Formula: C₆H₅ClN₄

InChI: InChI=1/C6H5ClN4/c1-3-4-5(9-2-8-4)11-6(7)10-3/h2,4H,1H3

9H-Purine, 2-chloro-6-methyl-

CAS: 1681-19-2

• Formula: C₆H₅ClN₄
• Purity: 98%
• Color and Shape: Solid
• Molecular weight: 168.5837

2-Chloro-6-methyl-9H-purine

CAS: 1681-19-2

• Purity: 95.0%
• Molecular weight: 168.5800018310547

2-Chloro-6-methyl-9H-purine

CAS: 1681-19-2

2-Chloro-6-methyl-9H-purine is an analog of purine nucleosides and nucleotides. It is used as a building …

• Formula: C₆H₅ClN₄
• Purity: Min. 95%
• Molecular weight: 168.58 g/mol