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Catalog Number:
17005
CAS Number:
213318-44-6
1-(tert-Butoxycarbonyl)indole-2-boronic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
1H-Indole-1-carboxylic acid, 2-borono-, 1,1-dimethylethyl ester
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Product Information

1-(tert-Butoxycarbonyl)indole-2-boronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valuable for its role in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in the development of complex organic molecules. Its unique structure, featuring a tert-butoxycarbonyl (Boc) protecting group, enhances its stability and reactivity, making it an ideal candidate for various applications in pharmaceutical research and development.

Researchers and industry professionals appreciate this compound for its ability to facilitate the synthesis of biologically active compounds, including potential drug candidates. Its compatibility with various functional groups allows for diverse modifications, enabling the creation of tailored molecules for specific therapeutic targets. Additionally, 1-(tert-Butoxycarbonyl)indole-2-boronic acid stands out due to its ease of handling and storage, making it a practical choice for laboratories focused on innovative chemical synthesis.

Synonyms
1H-Indole-1-carboxylic acid, 2-borono-, 1,1-dimethylethyl ester
CAS Number
213318-44-6
Purity
≥ 98% (HPLC)
Molecular Formula
C13H16BNO4
Molecular Weight
261.08
MDL Number
MFCD02093045
PubChem ID
2773302
Appearance
Pale yellow solid
Conditions
Store at 0-8°C
General Information
Synonyms
1H-Indole-1-carboxylic acid, 2-borono-, 1,1-dimethylethyl ester
CAS Number
213318-44-6
Purity
≥ 98% (HPLC)
Molecular Formula
C13H16BNO4
Molecular Weight
261.08
MDL Number
MFCD02093045
PubChem ID
2773302
Appearance
Pale yellow solid
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

1-(tert-Butoxycarbonyl)indole-2-boronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a crucial building block in the synthesis of pharmaceutical intermediates, particularly in the development of new anti-cancer agents.
  • Organic Synthesis: It is employed in various organic reactions, including Suzuki coupling, which is essential for forming carbon-carbon bonds in complex molecules.
  • Material Science: The compound is used in the creation of advanced materials, such as polymers and nanomaterials, enhancing properties like strength and thermal stability.
  • Bioconjugation: It plays a role in bioconjugation processes, allowing for the attachment of biomolecules to surfaces or other molecules, which is vital in drug delivery systems.
  • Analytical Chemistry: The compound is utilized in analytical methods to detect and quantify boron-containing compounds, aiding in environmental monitoring and quality control.

Citations