6,7-Dimethoxy-N²,N²-dimethylquinazoline-2,4-diamine is a chemical compound characterized by its quinazoline core structure, which is a bicyclic compound containing a benzene ring fused to a pyrimidine ring. This particular compound features two methoxy groups at the 6 and 7 positions, which can influence its solubility and reactivity. The presence of two dimethylamino groups at the N² positions enhances its basicity and may affect its interaction with biological targets. The compound is typically synthesized through multi-step organic reactions, and its properties may include moderate to high solubility in organic solvents, depending on the substituents. It may exhibit biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. As with many quinazoline derivatives, it could potentially interact with various enzymes or receptors, contributing to its pharmacological profile. Safety and handling precautions should be observed, as with any chemical substance, due to potential toxicity or reactivity.

6,7-dimethoxy-N~2~,N~2~-dimethylquinazoline-2,4-diamine

19216-68-3: 6,7-Dimethoxy-N²,N²-dimethylquinazoline-2,4-diamine is a chemical compound characterized by its quinazoline core structure, which is a bicyclic compound containing a benzene ring fused to a pyrimidine ring. This particular compound features two methoxy groups at the 6 and 7 positions, which can influence its solubility and reactivity. The presence of two dimethylamino groups at the N² positions enhances its basicity and may affect its interaction with biological targets. The compound is typically synthesized through multi-step organic reactions, and its properties may include moderate to high solubility in organic solvents, depending on the substituents. It may exhibit biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. As with many quinazoline derivatives, it could potentially interact with various enzymes or receptors, contributing to its pharmacological profile. Safety and handling precautions should be observed, as with any chemical substance, due to potential toxicity or reactivity.

Alfuzosin EP Impurity F

<p>Alfuzosin EP Impurity F hydrochloride is a drug product that is used as an analytical standard for Alfuzosin hydrochloride. It is a natural, synthetic, and impurity standard that exhibits similar chromatographic properties to the API. The CAS number of this impurity is 19216-68-3. This product has a niche market because it is used in metabolism studies. It also exhibits high purity and pharmacopoeia grade quality.</p>

CAS 19216-68-3

6,7-dimethoxy-N~2~,N~2~-dimethylquinazoline-2,4-diamine

Alfuzosin EP Impurity F

Ref: ST-EA-CP-A71006

Alfuzosin hydrochloride EP Impurity F hydrochloride

Ref: 3D-IA182629