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Catalog Number:
17733
CAS Number:
61272-71-7
5-Bromo- 1H -indazol-3-amina
Purity:
≥ 95 % (HPLC)
Synonym(s):
3-Amino-5-bromo-1 H -indazol
Documents
$43.87 /250 mg
Tamaño
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Product Information

5-Bromo-1H-indazol-3-amine is a versatile compound widely recognized for its applications in pharmaceutical research and development. This compound, characterized by its bromine substitution at the 5-position of the indazole ring, serves as a crucial building block in the synthesis of various bioactive molecules. Its unique structure allows it to interact with biological targets, making it an essential component in the development of novel therapeutic agents, particularly in oncology and neurology. Researchers have leveraged its properties to explore potential treatments for cancer and neurodegenerative diseases, showcasing its relevance in cutting-edge medicinal chemistry.

In addition to its pharmaceutical applications, 5-Bromo-1H-indazol-3-amine is also utilized in the development of agrochemicals and materials science. Its ability to act as a precursor in the synthesis of more complex compounds opens avenues for innovation in crop protection and advanced materials. The compound's stability and reactivity make it an attractive option for researchers looking to enhance the efficacy of their formulations. With its broad range of applications and potential for further exploration, 5-Bromo-1H-indazol-3-amine stands out as a valuable asset in both academic and industrial settings.

Synonyms
3-Amino-5-bromo-1 H -indazol
CAS Number
61272-71-7
Purity
≥ 95 % (HPLC)
Molecular Formula
C7H6BrN3
Molecular Weight
212.05
MDL Number
MFCD03426696
PubChem ID
817910
Appearance
Sólido de color blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
3-Amino-5-bromo-1 H -indazol
CAS Number
61272-71-7
Purity
≥ 95 % (HPLC)
Molecular Formula
C7H6BrN3
Molecular Weight
212.05
MDL Number
MFCD03426696
PubChem ID
817910
Appearance
Sólido de color blanquecino
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

5-Bromo-1H-indazol-3-amine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a crucial intermediate in the synthesis of various pharmaceutical agents, particularly in the development of anti-cancer drugs, due to its ability to inhibit specific protein kinases.
  • Biochemical Research: It is used in studies exploring signal transduction pathways, helping researchers understand cellular responses and the mechanisms of diseases.
  • Material Science: The compound finds applications in creating novel materials with specific electronic properties, which can be beneficial in the development of organic semiconductors.
  • Diagnostic Tools: 5-Bromo-1H-indazol-3-amine is employed in the creation of diagnostic assays, aiding in the detection of certain biomarkers associated with diseases.
  • Environmental Applications: It can be used in the synthesis of compounds for environmental monitoring, helping to detect pollutants and assess environmental health.

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