Therapeutic Uses
Anti-Cancer / Oncology
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
N-(2-Chloro-4-pyrimidinyl)-N,2,3-trimethyl-2H-indazol-6-amine, 444731-75-3
Application Notes
Useful research chemical for a range of applications
Purity by HPLC
Not less than 90%
Hazard Compound
No -Refer MSDS for accurate information
N-(2-Chloro-4-pyrimidinyl)-N,2,3-trimethyl-2H-indazol-6-amine is a drug product that is used as an analytical standard for HPLC, as well as in research and development of drugs.
Refund Policy
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N-(2-Chloro-4-pyrimidinyl)-N,2,3-trimethyl-2H-indazol-6-amine usage and description
N-(2-Chloro-4-pyrimidinyl)-N,2,3-trimethyl-2H-indazol-6-amine is a chemical compound that is used extensively in the pharmaceutical industry. It is a member of a class of compounds known as kinase inhibitors, which are designed to selectively target and inhibit the activity of specific enzymes involved in cellular signaling pathways. This particular compound is known to inhibit the activity of a specific kinase called Aurora A, which is involved in cell division and the regulation of mitosis.
In addition to its pharmaceutical applications, N-(2-Chloro-4-pyrimidinyl)-N,2,3-trimethyl-2H-indazol-6-amine is also used in the research setting as a tool compound to study the function of Aurora A and its role in various cellular processes. It is typically administered in vitro to cultured cells or in vivo to experimental animals, and its effects on cell proliferation, mitosis, and other cellular processes are carefully monitored.
Chemically, N-(2-Chloro-4-pyrimidinyl)-N,2,3-trimethyl-2H-indazol-6-amine is a small molecule with a molecular weight of 326.8 g/mol. Its molecular formula is C16H17ClN4, and it has a melting point of around 193-195°C. It is typically synthesized via a multi-step process involving the reaction of various starting materials under carefully controlled conditions. Its purity and identity are typically verified using a variety of analytical techniques, including HPLC, mass spectrometry, and NMR spectroscopy.
