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Catalog Number:
18842
CAS Number:
433969-29-0
3-(Boc-aminomethyl)pyridine-4-boronic acid
Purity:
≥ 97% (HPLC)
Synonym(s):
(3-([(tert-Butoxycarbonyl)amino]methyl)pyridin-4-yl)boronic acid
Documents
$168.35 /100MG
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Product Information

3-(Boc-aminomethyl)pyridine-4-boronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and reactivity, making it an ideal candidate for various coupling reactions, particularly in the formation of carbon-nitrogen bonds. Its unique structure allows for applications in the development of pharmaceuticals, agrochemicals, and advanced materials. Researchers have leveraged this compound in the synthesis of complex molecules, including biologically active compounds and inhibitors, showcasing its importance in drug discovery and development.

The compound's boronic acid functionality also enables its use in Suzuki-Miyaura cross-coupling reactions, a key method in the formation of biaryl compounds, which are essential in many therapeutic agents. With its favorable properties, 3-(Boc-aminomethyl)pyridine-4-boronic acid stands out as a valuable tool for chemists seeking to innovate and streamline their synthetic pathways, ultimately contributing to advancements in various fields, including pharmaceuticals and material science.

Synonyms
(3-([(tert-Butoxycarbonyl)amino]methyl)pyridin-4-yl)boronic acid
CAS Number
433969-29-0
Purity
≥ 97% (HPLC)
Molecular Formula
C11H17BN2O4
Molecular Weight
252.07
MDL Number
MFCD05664023
PubChem ID
10999519
Appearance
White to off-white powder
Conditions
Store at 0-8 °C
General Information
Synonyms
(3-([(tert-Butoxycarbonyl)amino]methyl)pyridin-4-yl)boronic acid
CAS Number
433969-29-0
Purity
≥ 97% (HPLC)
Molecular Formula
C11H17BN2O4
Molecular Weight
252.07
MDL Number
MFCD05664023
PubChem ID
10999519
Appearance
White to off-white powder
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

3-(Boc-aminomethyl)pyridine-4-boronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of targeted therapies for cancer treatment.
  • Bioconjugation: It is employed in bioconjugation processes to attach biomolecules to surfaces or other molecules, enhancing the efficacy of drug delivery systems.
  • Catalysis: The compound acts as a catalyst in organic reactions, improving reaction rates and selectivity, which is crucial in the production of fine chemicals.
  • Material Science: It is used in the development of advanced materials, such as sensors and polymers, due to its unique boronic acid functionality that allows for specific interactions with sugars.
  • Research in Medicinal Chemistry: This compound is a valuable tool for medicinal chemists exploring new drug candidates, particularly those targeting specific biological pathways.

Citations