7-Bromothieno[3,2-d]pyrimidin-4-amine is a heterocyclic organic compound characterized by the presence of a thieno-pyrimidine structure, which incorporates both sulfur and nitrogen atoms in its ring system. The compound features a bromine substituent at the 7-position of the thieno ring and an amino group at the 4-position of the pyrimidine moiety. This unique arrangement contributes to its potential biological activity, making it of interest in medicinal chemistry and drug development. The presence of the bromine atom can enhance the compound's reactivity and influence its interaction with biological targets. Additionally, the thieno and pyrimidine rings provide a planar structure that may facilitate stacking interactions with nucleic acids or proteins. The compound's solubility and stability can vary depending on the solvent and environmental conditions, which are important factors to consider in its applications. Overall, 7-bromothieno[3,2-d]pyrimidin-4-amine represents a versatile scaffold for further chemical modifications and exploration in pharmaceutical research.

7-bromothieno[3,2-d]pyrimidin-4-amine

1318133-32-2: 7-Bromothieno[3,2-d]pyrimidin-4-amine is a heterocyclic organic compound characterized by the presence of a thieno-pyrimidine structure, which incorporates both sulfur and nitrogen atoms in its ring system. The compound features a bromine substituent at the 7-position of the thieno ring and an amino group at the 4-position of the pyrimidine moiety. This unique arrangement contributes to its potential biological activity, making it of interest in medicinal chemistry and drug development. The presence of the bromine atom can enhance the compound's reactivity and influence its interaction with biological targets. Additionally, the thieno and pyrimidine rings provide a planar structure that may facilitate stacking interactions with nucleic acids or proteins. The compound's solubility and stability can vary depending on the solvent and environmental conditions, which are important factors to consider in its applications. Overall, 7-bromothieno[3,2-d]pyrimidin-4-amine represents a versatile scaffold for further chemical modifications and exploration in pharmaceutical research.

Thieno[3,2-d]pyrimidin-4-amine, 7-bromo-

<p>7-Bromothieno[3,2-d]pyrimidin-4-amine</p>

CAS 1318133-32-2

7-bromothieno[3,2-d]pyrimidin-4-amine

Thieno[3,2-d]pyrimidin-4-amine, 7-bromo-

Ref: IN-DA000ZRU

7-Bromothieno[3,2-d]pyrimidin-4-amine

Ref: 54-OR1021916

7-Bromothieno[3,2-d]pyrimidin-4-amine

Ref: 10-F320922

7-Bromothieno[3,2-d]pyrimidin-4-amine

Ref: 3D-TCC13332