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Catalog Number:
19507
CAS Number:
96541-83-2
Quinoline-5-carboxylic acid hydrazide
Purity:
≥ 95% (HPLC)
Synonym(s):
Quinoline-5-carbohydrazide
Documents
$103.56 /250MG
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Product Information

Quinoline-5-carboxylic acid hydrazide is a versatile compound with significant applications in pharmaceuticals and organic synthesis. This hydrazide derivative of quinoline exhibits unique properties that make it valuable in the development of various bioactive molecules. Its structure allows for the formation of diverse derivatives, which can be tailored for specific biological activities, making it a crucial intermediate in drug discovery and development. Researchers have utilized Quinoline-5-carboxylic acid hydrazide in the synthesis of potential antimicrobial and anticancer agents, showcasing its relevance in medicinal chemistry.

In addition to its pharmaceutical applications, Quinoline-5-carboxylic acid hydrazide is also employed in the preparation of agrochemicals and dyes, highlighting its versatility across different industries. Its ability to form stable complexes with metal ions further enhances its utility in catalysis and material science. With its promising applications and the potential for further exploration, Quinoline-5-carboxylic acid hydrazide stands out as a compound of interest for researchers and industry professionals seeking innovative solutions.

Synonyms
Quinoline-5-carbohydrazide
CAS Number
96541-83-2
Purity
≥ 95% (HPLC)
Molecular Formula
C10H9N3O
Molecular Weight
187.2
MDL Number
MFCD01063087
PubChem ID
43237126
Appearance
Light brown to off-white solid
Conditions
Store at 0-8 °C
General Information
Synonyms
Quinoline-5-carbohydrazide
CAS Number
96541-83-2
Purity
≥ 95% (HPLC)
Molecular Formula
C10H9N3O
Molecular Weight
187.2
MDL Number
MFCD01063087
PubChem ID
43237126
Appearance
Light brown to off-white solid
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Quinoline-5-carboxylic acid hydrazide is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in synthesizing various pharmaceuticals, particularly in developing anti-inflammatory and antimicrobial agents.
  • Biological Research: It is used in studies investigating the mechanisms of action of certain drugs, helping researchers understand how compounds interact at the molecular level.
  • Analytical Chemistry: Quinoline-5-carboxylic acid hydrazide is employed as a reagent in analytical methods, aiding in the detection and quantification of metals in environmental samples.
  • Material Science: The compound is explored for its potential use in creating novel materials with specific properties, such as enhanced thermal stability and conductivity.
  • Agrochemical Applications: It is being studied for its effectiveness in developing new agrochemicals, particularly those aimed at pest control and plant growth regulation.

Citations