2-Chloro-5-methyl-thieno[2,3-d]pyrimidine is a heterocyclic compound characterized by its fused thieno and pyrimidine rings, which contribute to its unique chemical properties. The presence of a chlorine atom at the second position and a methyl group at the fifth position of the pyrimidine ring influences its reactivity and solubility. This compound typically exhibits moderate polarity due to the electronegative chlorine atom, which can participate in various chemical reactions, including nucleophilic substitutions. It is often utilized in medicinal chemistry and drug development due to its potential biological activity, particularly in the field of anti-cancer and anti-inflammatory agents. The thieno-pyrimidine framework is known for its ability to interact with biological targets, making it a subject of interest in pharmaceutical research. Additionally, its stability under standard laboratory conditions allows for various synthetic modifications, enhancing its utility in organic synthesis. Overall, 2-chloro-5-methyl-thieno[2,3-d]pyrimidine represents a versatile scaffold in the development of novel therapeutic compounds.

2-chloro-5-methyl-thieno[2,3-d]pyrimidine

83259-31-8: 2-Chloro-5-methyl-thieno[2,3-d]pyrimidine is a heterocyclic compound characterized by its fused thieno and pyrimidine rings, which contribute to its unique chemical properties. The presence of a chlorine atom at the second position and a methyl group at the fifth position of the pyrimidine ring influences its reactivity and solubility. This compound typically exhibits moderate polarity due to the electronegative chlorine atom, which can participate in various chemical reactions, including nucleophilic substitutions. It is often utilized in medicinal chemistry and drug development due to its potential biological activity, particularly in the field of anti-cancer and anti-inflammatory agents. The thieno-pyrimidine framework is known for its ability to interact with biological targets, making it a subject of interest in pharmaceutical research. Additionally, its stability under standard laboratory conditions allows for various synthetic modifications, enhancing its utility in organic synthesis. Overall, 2-chloro-5-methyl-thieno[2,3-d]pyrimidine represents a versatile scaffold in the development of novel therapeutic compounds.

CAS 83259-31-8

2-chloro-5-methyl-thieno[2,3-d]pyrimidine

2-Chloro-5-methylthieno[2,3-d]pyrimidine

Ref: IN-DA003GZA

2-Chloro-5-methylthieno[2,3-d]pyrimidine

Ref: 10-F621345