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Catalog Number:
19115
CAS Number:
310886-79-4
Éster metílico del ácido 5-fluoro-1 H -indol-3-carboxílico
Purity:
≥ 97 % (HPLC)
Synonym(s):
5-Fluoro- 1H- indol-3-carboxilato de metilo
Documents
$43.87 /100 mg
Tamaño
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Product Information

5-Fluoro-1H-indole-3-carboxylic acid methyl ester is a versatile compound known for its significant role in pharmaceutical research and development. This methyl ester derivative of 5-fluoroindole-3-carboxylic acid exhibits unique properties that make it an essential building block in the synthesis of various biologically active molecules. Its fluorine substitution enhances the compound's lipophilicity and metabolic stability, making it particularly valuable in drug design and medicinal chemistry. Researchers utilize this compound in the development of novel therapeutic agents, especially in oncology and neurology, where indole derivatives have shown promising activity against various cancer cell lines and neurological disorders.

In addition to its pharmaceutical applications, 5-Fluoro-1H-indole-3-carboxylic acid methyl ester serves as an important intermediate in organic synthesis, allowing for the creation of complex molecular architectures. Its ability to undergo various chemical transformations opens up pathways for the development of new materials and agrochemicals. With its favorable properties and diverse applications, this compound is a key asset for researchers and industry professionals looking to innovate in their respective fields.

Synonyms
5-Fluoro- 1H- indol-3-carboxilato de metilo
CAS Number
310886-79-4
Purity
≥ 97 % (HPLC)
Molecular Formula
C10H8FNO2
Molecular Weight
193.18
MDL Number
MFCD06203952
PubChem ID
34176452
Appearance
Polvo de color amarillo parduzco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
5-Fluoro- 1H- indol-3-carboxilato de metilo
CAS Number
310886-79-4
Purity
≥ 97 % (HPLC)
Molecular Formula
C10H8FNO2
Molecular Weight
193.18
MDL Number
MFCD06203952
PubChem ID
34176452
Appearance
Polvo de color amarillo parduzco
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-Fluoro-1H-indole-3-carboxylic acid methyl ester 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-cancer agents, due to its unique fluorinated structure that enhances biological activity.
  • Biochemical Research: It is used in studies exploring the mechanisms of action of indole derivatives, helping researchers understand their role in cellular processes and potential therapeutic effects.
  • Material Science: The compound is explored for its potential applications in creating novel materials, such as organic semiconductors, which are essential in the development of electronic devices.
  • Agrochemicals: It can be utilized in the synthesis of agrochemical products, contributing to the development of more effective pesticides and herbicides that target specific pests while minimizing environmental impact.
  • Fluorine Chemistry: This compound is significant in fluorine chemistry research, where it aids in the exploration of new fluorinated compounds that exhibit improved properties over non-fluorinated analogs, such as increased stability and bioactivity.

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