CAS 92434-13-4

N-(6-Chloro-4-phenylquinazolin-2-yl)guanidine

Description:

N-(6-Chloro-4-phenylquinazolin-2-yl)guanidine is a chemical compound characterized by its unique structure, which includes a quinazoline core substituted with a chloro group and a phenyl group, along with a guanidine moiety. This compound typically exhibits properties associated with heterocyclic compounds, such as potential biological activity, making it of interest in medicinal chemistry. The presence of the chloro substituent can influence its reactivity and solubility, while the guanidine group may contribute to its basicity and ability to form hydrogen bonds. Such compounds are often investigated for their pharmacological properties, including antitumor and antimicrobial activities. Additionally, the molecular interactions facilitated by the quinazoline structure can lead to various applications in drug development. As with many chemical substances, safety and handling precautions are essential, given the potential toxicity associated with halogenated compounds. Overall, N-(6-Chloro-4-phenylquinazolin-2-yl)guanidine represents a class of compounds that bridges organic chemistry and pharmacology.

Formula: C₁₅H₁₂ClN₅

Synonyms:

• 1-(6-Chloro-4-phenylquinazolin-2-yl)guanidine
• NHE3-IN-2
• N-(6-Chloro-4-phenylquinazolin-2-yl)guanidine

N-(6-Chloro-4-phenylquinazolin-2-yl)guanidine

Controlled Product

CAS: 92434-13-4

Formula: C₁₅H₁₂ClN₅

Color and Shape: Neat

Molecular weight: 297.742

Ref: TR-N063545

N-(6-Chloro-4-phenylquinazolin-2-yl)guanidine-d5

Controlled Product

CAS: 92434-13-4

Formula: C₁₅D₅H₇ClN₅

Color and Shape: Neat

Molecular weight: 302.773

Ref: TR-N063544

NHE3-IN-2

CAS: 92434-13-4

NHE3-IN-2 is an inhibitor of NHE3 (Na+/H+ exchanger-3), applicable for treating hypertension, thrombosis, and ischaemic diseases.

Formula: C₁₅H₁₂ClN₅

Color and Shape: Solid

Molecular weight: 297.74

Ref: TM-T60652