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Catalog Number:
17288
CAS Number:
78155-76-7
Ácido 5-nitro-1 H -indazol-3-carboxílico
Purity:
≥ 95% (RMN)
Synonym(s):
Ácido 5-nitro-3-(1 H indazol carboxílico, Ácido 5-nitro indazol carboxílico
Documents
$117.78 /250 mg
Tamaño
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Product Information

5-Nitro-1H-indazole-3-carboxylic acid is a versatile compound recognized for its significant role in pharmaceutical and chemical research. This compound, characterized by its nitro and carboxylic acid functional groups, exhibits unique properties that make it a valuable intermediate in the synthesis of various bioactive molecules. Researchers utilize 5-Nitro-1H-indazole-3-carboxylic acid in the development of novel pharmaceuticals, particularly in the creation of anti-inflammatory and antimicrobial agents. Its ability to participate in diverse chemical reactions enhances its utility in organic synthesis, allowing for the efficient construction of complex molecular architectures.

Additionally, this compound serves as a crucial building block in the field of agrochemicals, contributing to the formulation of effective herbicides and pesticides. Its stability and reactivity profile make it an attractive option for researchers looking to innovate within these sectors. With its broad applicability and potential to facilitate advancements in drug discovery and agricultural chemistry, 5-Nitro-1H-indazole-3-carboxylic acid stands out as a compound of interest for professionals aiming to enhance their research and product development efforts.

Synonyms
Ácido 5-nitro-3-(1 H indazol carboxílico, Ácido 5-nitro indazol carboxílico
CAS Number
78155-76-7
Purity
≥ 95% (RMN)
Molecular Formula
C8H5N3O4
Molecular Weight
207.15
MDL Number
MFCD05663993
PubChem ID
7144652
Appearance
Sólido incoloro a amarillo
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido 5-nitro-3-(1 H indazol carboxílico, Ácido 5-nitro indazol carboxílico
CAS Number
78155-76-7
Purity
≥ 95% (RMN)
Molecular Formula
C8H5N3O4
Molecular Weight
207.15
MDL Number
MFCD05663993
PubChem ID
7144652
Appearance
Sólido incoloro a amarillo
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-Nitro-1H-indazole-3-carboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is explored for its potential as an anti-inflammatory agent, making it valuable in the development of new medications for chronic inflammatory diseases.
  • Biochemical Research: It serves as a useful tool in studying enzyme inhibition, particularly in the context of cancer research, where understanding enzyme activity can lead to new therapeutic strategies.
  • Analytical Chemistry: The compound is employed in the synthesis of various derivatives, which can be used as standards in analytical methods, enhancing the accuracy of chemical analysis in laboratories.
  • Agricultural Chemistry: It is being investigated for its potential applications in developing new agrochemicals, particularly those aimed at pest control, which can lead to more effective and environmentally friendly solutions.
  • Material Science: Researchers are exploring its properties for use in creating novel materials, such as polymers or coatings, that require specific chemical functionalities for enhanced performance.

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