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Catalog Number:
12837
CAS Number:
135884-31-0
Boc-2-pyrryl-boronic acid
Purity:
≥ 97%
Synonym(s):
N-Boc-2-pyrroleboronic acid
Documents
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Product Information

Boc-2-pyrryl-boronic acid is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound 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-carbon bonds. Its unique structure allows for selective functionalization, enabling researchers to create complex molecules with precision.

In the pharmaceutical industry, Boc-2-pyrryl-boronic acid is utilized in the development of novel therapeutic agents, particularly in the synthesis of biologically active compounds. Its ability to participate in Suzuki-Miyaura cross-coupling reactions makes it invaluable for constructing intricate molecular architectures. Additionally, its favorable solubility and compatibility with various reaction conditions further enhance its appeal to chemists seeking efficient pathways for compound synthesis. This compound stands out for its potential to streamline synthetic processes while delivering high yields, making it a preferred choice for both academic and industrial applications.

Synonyms
N-Boc-2-pyrroleboronic acid
CAS Number
135884-31-0
Purity
≥ 97%
Molecular Formula
C9H14BNO4
Molecular Weight
211.02
MDL Number
MFCD01318939
PubChem ID
2734321
Appearance
Gray to purple solid
Conditions
Store at 0 - 8 °C
General Information
Synonyms
N-Boc-2-pyrroleboronic acid
CAS Number
135884-31-0
Purity
≥ 97%
Molecular Formula
C9H14BNO4
Molecular Weight
211.02
MDL Number
MFCD01318939
PubChem ID
2734321
Appearance
Gray to purple 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

Boc-2-pyrryl-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 boron-containing drugs that target specific biological pathways.
  • Organic Synthesis: It is employed in cross-coupling reactions, allowing chemists to create complex organic molecules efficiently, which is crucial in the fields of materials science and agrochemicals.
  • Bioconjugation: The unique reactivity of boronic acids makes it useful for attaching biomolecules to surfaces or other molecules, facilitating advancements in biochemistry and molecular biology.
  • Sensor Technology: This compound can be used in the development of sensors for detecting sugars and other biomolecules, benefiting industries focused on diagnostics and environmental monitoring.
  • Catalysis: It acts as a catalyst in various chemical reactions, enhancing reaction rates and selectivity, which is particularly advantageous in fine chemical production and green chemistry initiatives.

Citations