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Catalog Number:
19087
CAS Number:
10406-06-1
Ácido 5-bromo-1 H -indol-3-carboxílico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ácido 5-bromoindol-3-carboxílico
Documents
$43.87 /250 mg
Tamaño
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Product Information

5-Bromo-1H-indole-3-carboxylic acid is a versatile compound widely utilized in organic synthesis and pharmaceutical research. This compound features a bromine atom at the 5-position of the indole ring, which enhances its reactivity and makes it an essential building block in the development of various bioactive molecules. Its unique structure allows for the introduction of diverse functional groups, facilitating the synthesis of complex compounds that are crucial in medicinal chemistry.

Researchers and industry professionals often leverage 5-Bromo-1H-indole-3-carboxylic acid in the design of novel pharmaceuticals, particularly in the development of anti-cancer agents and other therapeutic compounds. Its application extends to the synthesis of indole derivatives, which are known for their significant biological activities, including anti-inflammatory and antimicrobial properties. The compound's ability to serve as a precursor in the synthesis of more complex molecules makes it an invaluable resource in both academic and industrial laboratories, driving innovation in drug discovery and development.

Synonyms
Ácido 5-bromoindol-3-carboxílico
CAS Number
10406-06-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C9H6BrNO2
Molecular Weight
240.06
MDL Number
MFCD05664007
PubChem ID
7018243
Appearance
Polvo de color blanco a rosa
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido 5-bromoindol-3-carboxílico
CAS Number
10406-06-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C9H6BrNO2
Molecular Weight
240.06
MDL Number
MFCD05664007
PubChem ID
7018243
Appearance
Polvo de color blanco a rosa
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-Bromo-1H-indole-3-carboxylic acid 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 drugs targeting neurological disorders.
  • Biochemical Research: It is used in studies related to enzyme inhibition and receptor binding, helping researchers understand biological pathways and mechanisms.
  • Organic Synthesis: The compound is a valuable building block in organic chemistry, facilitating the creation of more complex molecules in the lab.
  • Material Science: It finds applications in the development of new materials, such as polymers and coatings, due to its unique chemical properties.
  • Agricultural Chemistry: 5-Bromo-1H-indole-3-carboxylic acid is explored for its potential use in agrochemicals, contributing to the formulation of effective pesticides and herbicides.

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