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Catalog Number:
31273
CAS Number:
23100-12-1
6-chloropyridine-3-carboxaldéhyde
Purity:
≥ 98 % (RMN)
Synonym(s):
2-Chloro-5-pyridinecarboxaldéhyde, 2-Chloro-5-formylpyridine
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Product Information

6-Chloropyridine-3-carboxaldehyde is a versatile chemical compound widely utilized in the synthesis of various pharmaceuticals and agrochemicals. This compound, characterized by its unique chloropyridine structure, serves as a crucial intermediate in the production of biologically active molecules, including potential anti-inflammatory and anti-cancer agents. Its reactivity allows for easy functionalization, making it an essential building block for researchers and industry professionals looking to develop novel compounds with specific therapeutic properties.

In addition to its applications in medicinal chemistry, 6-Chloropyridine-3-carboxaldehyde is also employed in the synthesis of specialty chemicals and fine chemicals, enhancing its relevance in the agrochemical sector. Its ability to undergo various chemical transformations enables the creation of diverse derivatives, which can be tailored for specific applications. The compound's stability and ease of handling further contribute to its appeal, making it a preferred choice for laboratories and manufacturing processes alike.

Synonyms
2-Chloro-5-pyridinecarboxaldéhyde, 2-Chloro-5-formylpyridine
CAS Number
23100-12-1
Purity
≥ 98 % (RMN)
Molecular Formula
C6H4ClNO
Molecular Weight
141.56
MDL Number
MFCD03095223
PubChem ID
2764053
Melting Point
81 - 83 ?C
Appearance
Solide violet
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
2-Chloro-5-pyridinecarboxaldéhyde, 2-Chloro-5-formylpyridine
CAS Number
23100-12-1
Purity
≥ 98 % (RMN)
Molecular Formula
C6H4ClNO
Molecular Weight
141.56
MDL Number
MFCD03095223
PubChem ID
2764053
Melting Point
81 - 83 ?C
Appearance
Solide violet
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

6-Chloropyridine-3-carboxaldehyde is widely utilized in research focused on:

  • Synthesis of Pharmaceuticals: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders and infections.
  • Agricultural Chemicals: It is used in the development of agrochemicals, including herbicides and fungicides, enhancing crop protection and yield.
  • Material Science: The compound finds applications in creating specialized polymers and materials, contributing to advancements in coatings and adhesives.
  • Research in Organic Chemistry: It acts as a building block for complex organic molecules, facilitating research in synthetic methodologies and reaction mechanisms.
  • Fluorescent Probes: 6-Chloropyridine-3-carboxaldehyde is utilized in the design of fluorescent probes for biological imaging, aiding in cellular studies and diagnostics.

Citations