956200-57-0

Basic information

• Product Name: 4-(4-AMINO-5-METHYL-1H-PYRAZOL-1-YL)BENZOIC ACID
• Synonyms: 4-(4-AMINO-5-METHYL-1H-PYRAZOL-1-YL)BENZOIC ACID
• CAS NO: 956200-57-0
• Molecular Formula: C11H11N3O2
• Molecular Weight: 217.22
• Mol File: 956200-57-0.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-(4-AMINO-5-METHYL-1H-PYRAZOL-1-YL)BENZOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-AMINO-5-METHYL-1H-PYRAZOL-1-YL)BENZOIC ACID(956200-57-0)
• EPA Substance Registry System: 4-(4-AMINO-5-METHYL-1H-PYRAZOL-1-YL)BENZOIC ACID(956200-57-0)

Safety Data

• Hazardous Substances Data: 956200-57-0(Hazardous Substances Data)

Usage

Description

4-(4-AMINO-5-METHYL-1H-PYRAZOL-1-YL)BENZOIC ACID is a chemical compound that serves as an analog of 3-(5-Amino-3-methyl-1H-pyrazol-1-yl)benzoic Acid (A617505, HCl). It is characterized by its unique molecular structure, which features a pyrazole ring fused to a benzene ring, and possesses an amino group and a methyl group attached to the pyrazole moiety. 4-(4-AMINO-5-METHYL-1H-PYRAZOL-1-YL)BENZOIC ACID is known for its potential applications in the synthesis of quinoline derivatives and as a reagent in the development of caspase-3 inhibitors.

Uses

Used in Pharmaceutical Industry:
4-(4-AMINO-5-METHYL-1H-PYRAZOL-1-YL)BENZOIC ACID is used as a reagent in the synthesis of quinoline derivatives, which are known for their diverse range of biological activities and potential therapeutic applications. These quinoline-based compounds can be further modified and optimized to develop new drugs with improved pharmacological properties.
Used in Caspase-3 Inhibitor Development:
4-(4-AMINO-5-METHYL-1H-PYRAZOL-1-YL)BENZOIC ACID is utilized in the development of caspase-3 inhibitors, which are important for understanding the molecular mechanisms of apoptosis and for the discovery of potential therapeutic agents targeting this process. Caspase-3 is a key enzyme involved in the execution phase of apoptosis, and its inhibition can provide valuable insights into the regulation of cell death and survival pathways.