Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
21583
CAS Number:
827-01-0
5-Cloroindol-3-carboxaldehído
Purity:
≥ 98%
Synonym(s):
5-Cloro- 1H- indol-3-carbaldehído
Documents
$36.65 /1G
Tamaño
Request Bulk Quote
Product Information

5-Chloroindole-3-carboxaldehyde is a versatile compound widely recognized for its applications in organic synthesis and pharmaceutical research. This compound, characterized by its unique chlorinated indole structure, serves as a crucial intermediate in the synthesis of various biologically active molecules. Its reactivity allows for the introduction of diverse functional groups, making it an essential building block in the development of novel pharmaceuticals, particularly in the field of medicinal chemistry. Researchers have utilized 5-Chloroindole-3-carboxaldehyde in the synthesis of indole-based compounds, which have shown promising activity against a range of diseases, including cancer and neurological disorders.

In addition to its pharmaceutical applications, 5-Chloroindole-3-carboxaldehyde is also valuable in the production of agrochemicals and dyes, where its unique properties enhance the efficacy and stability of formulations. Its ability to undergo various chemical transformations makes it a preferred choice for chemists looking to innovate and optimize their synthetic pathways. With its broad applicability and significant potential, 5-Chloroindole-3-carboxaldehyde stands out as a key compound for researchers and industry professionals aiming to advance their projects in drug development and chemical synthesis.

Synonyms
5-Cloro- 1H- indol-3-carbaldehído
CAS Number
827-01-0
Purity
≥ 98%
Molecular Formula
C9H6ClNO
Molecular Weight
179.61
MDL Number
MFCD00175291
PubChem ID
2795374
Appearance
Sólido de color amarillo a beige
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
5-Cloro- 1H- indol-3-carbaldehído
CAS Number
827-01-0
Purity
≥ 98%
Molecular Formula
C9H6ClNO
Molecular Weight
179.61
MDL Number
MFCD00175291
PubChem ID
2795374
Appearance
Sólido de color amarillo a beige
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

5-Chloroindole-3-carboxaldehyde is widely utilized in research focused on:

  • Synthesis of Pharmaceuticals: This compound serves as an important intermediate in the synthesis of various pharmaceutical agents, particularly in developing drugs that target neurological disorders.
  • Fluorescent Probes: It is used to create fluorescent probes for biological imaging, allowing researchers to visualize cellular processes in real-time, which is crucial in drug discovery and development.
  • Organic Synthesis: The compound is a valuable building block in organic chemistry, facilitating the synthesis of complex molecules with potential applications in materials science and nanotechnology.
  • Biochemical Research: It plays a role in studying enzyme activities and metabolic pathways, aiding researchers in understanding disease mechanisms and developing therapeutic strategies.
  • Material Development: The compound is explored for its potential in developing new materials with unique electronic properties, which can be beneficial in the fields of electronics and photonics.

Citas