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Catalog Number:
17741
CAS Number:
1077-96-9
5-Fluoro-1H-indazole-3-carboxylic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
5-Fluoro-3-indazolecarboxylic acid
Documents
$51.18 /250MG
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Product Information

5-Fluoro-1H-indazole-3-carboxylic acid is a versatile compound recognized for its significant role in pharmaceutical research and development. This compound, characterized by its unique fluorine substitution, offers enhanced biological activity, making it a valuable building block in the synthesis of various bioactive molecules. Its structure allows for the exploration of novel therapeutic agents, particularly in the fields of oncology and neurology, where it can be utilized in the development of targeted treatments. Researchers have noted its potential in modulating specific biological pathways, which can lead to innovative solutions in drug design.

In addition to its pharmaceutical applications, 5-Fluoro-1H-indazole-3-carboxylic acid is also relevant in agrochemical formulations, where it can contribute to the development of new crop protection agents. Its ability to interact with biological systems opens avenues for creating environmentally friendly pesticides that are effective yet safe. The compound's unique properties, such as its stability and reactivity, make it an attractive option for researchers and industry professionals looking to enhance their product offerings or explore new research avenues.

Synonyms
5-Fluoro-3-indazolecarboxylic acid
CAS Number
1077-96-9
Purity
≥ 99% (HPLC)
Molecular Formula
C8H5FN2O2
Molecular Weight
180.14
MDL Number
MFCD03840628
PubChem ID
14999052
Appearance
Yellow solid
Conditions
Store at 0-8 °C
General Information
Synonyms
5-Fluoro-3-indazolecarboxylic acid
CAS Number
1077-96-9
Purity
≥ 99% (HPLC)
Molecular Formula
C8H5FN2O2
Molecular Weight
180.14
MDL Number
MFCD03840628
PubChem ID
14999052
Appearance
Yellow solid
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

5-Fluoro-1H-indazole-3-carboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents, due to its ability to inhibit specific enzymes involved in tumor growth.
  • Agricultural Chemistry: It is used in the formulation of agrochemicals, providing effective solutions for pest control and crop protection, thereby enhancing agricultural productivity.
  • Biochemical Research: Researchers employ this compound in studies related to enzyme activity and metabolic pathways, helping to unravel complex biological processes.
  • Material Science: The compound is explored for its potential in creating novel materials with unique properties, such as improved thermal stability and electrical conductivity.
  • Analytical Chemistry: It is utilized as a reference standard in analytical methods, ensuring accurate detection and quantification of related compounds in various samples.

Citations