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Catalog Number:
19505
CAS Number:
29620-62-0
Hidrazida del ácido quinolin-4-carboxílico
Purity:
≥ 95 % (HPLC)
Synonym(s):
Quinolina-4-carbohidrazida
Documents
$180.27 /250 mg
Tamaño
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Product Information

Quinoline-4-carboxylic acid hydrazide is a versatile compound recognized for its significant role in various chemical and pharmaceutical applications. This hydrazide derivative of quinoline exhibits unique properties that make it valuable in the synthesis of bioactive molecules, particularly in the development of pharmaceuticals targeting infectious diseases and cancer. Its ability to act as a building block in organic synthesis allows researchers to explore new therapeutic avenues, enhancing drug efficacy and specificity.

Additionally, Quinoline-4-carboxylic acid hydrazide is utilized in the preparation of ligands for coordination chemistry, contributing to advancements in materials science and catalysis. Its stability and reactivity under various conditions make it an ideal candidate for researchers looking to innovate in drug design and development. The compound's potential to form complexes with metal ions further broadens its application scope, making it a crucial component in the formulation of advanced materials and catalysts.

Synonyms
Quinolina-4-carbohidrazida
CAS Number
29620-62-0
Purity
≥ 95 % (HPLC)
Molecular Formula
C10H9N3O
Molecular Weight
187.2
MDL Number
MFCD00784841
PubChem ID
3011577
Appearance
Gris pálido sólido
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Quinolina-4-carbohidrazida
CAS Number
29620-62-0
Purity
≥ 95 % (HPLC)
Molecular Formula
C10H9N3O
Molecular Weight
187.2
MDL Number
MFCD00784841
PubChem ID
3011577
Appearance
Gris pálido sólido
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

Quinoline-4-carboxylic acid hydrazide 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-inflammatory and antimicrobial agents.
  • Biological Research: It is used in studies investigating enzyme inhibition and receptor interactions, providing insights into disease mechanisms and potential therapeutic targets.
  • Material Science: The compound is explored for its properties in creating novel materials, including polymers and coatings, which can enhance durability and performance.
  • Agricultural Chemistry: Quinoline-4-carboxylic acid hydrazide is investigated for its potential as a pesticide or herbicide, contributing to sustainable agricultural practices.
  • Analytical Chemistry: It is employed in analytical methods for detecting and quantifying specific compounds, aiding in quality control and regulatory compliance in various industries.

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