2-(Chloromethyl)-5-methylthieno[2,3-d]pyrimidin-4(3H)-one is a heterocyclic compound characterized by its unique thieno-pyrimidine structure, which incorporates both sulfur and nitrogen atoms in its ring system. This compound features a chloromethyl group, which enhances its reactivity and potential for further chemical modifications. The presence of a methyl group at the 5-position contributes to its hydrophobic characteristics, influencing its solubility and interaction with biological systems. The thieno[2,3-d]pyrimidin-4(3H)-one core is known for its biological activity, often serving as a scaffold in medicinal chemistry for the development of pharmaceuticals. The compound's molecular structure suggests potential applications in drug discovery, particularly in targeting specific biological pathways. Additionally, the chloromethyl group can facilitate nucleophilic substitution reactions, making it a versatile intermediate in organic synthesis. Overall, this compound exemplifies the complexity and utility of heterocyclic chemistry in developing novel therapeutic agents.

2-(chloromethyl)-5-methylthieno[2,3-d]pyrimidin-4(3H)-one

568577-81-1: 2-(Chloromethyl)-5-methylthieno[2,3-d]pyrimidin-4(3H)-one is a heterocyclic compound characterized by its unique thieno-pyrimidine structure, which incorporates both sulfur and nitrogen atoms in its ring system. This compound features a chloromethyl group, which enhances its reactivity and potential for further chemical modifications. The presence of a methyl group at the 5-position contributes to its hydrophobic characteristics, influencing its solubility and interaction with biological systems. The thieno[2,3-d]pyrimidin-4(3H)-one core is known for its biological activity, often serving as a scaffold in medicinal chemistry for the development of pharmaceuticals. The compound's molecular structure suggests potential applications in drug discovery, particularly in targeting specific biological pathways. Additionally, the chloromethyl group can facilitate nucleophilic substitution reactions, making it a versatile intermediate in organic synthesis. Overall, this compound exemplifies the complexity and utility of heterocyclic chemistry in developing novel therapeutic agents.

CAS 568577-81-1

2-(chloromethyl)-5-methylthieno[2,3-d]pyrimidin-4(3H)-one

2-(Chloromethyl)-5-methylthieno[2,3-d]pyrimidin-4(3H)-one

Ref: IN-DA00EE55

2-(Chloromethyl)-5-methylthieno[2,3-d]pyrimidin-4(3H)-one

Ref: 54-OR1074745