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Catalog Number:
40171
CAS Number:
389621-81-2
4-[(1-Pyrrolidinyl)carbonyl]phenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
4-[(1-Pyrrolidinyl)carbonyl]benzeneboronic acid
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Product Information

4-[(1-Pyrrolidinyl)carbonyl]phenylboronic acid is a versatile compound widely recognized for its applications in medicinal chemistry and organic synthesis. This boronic acid derivative features a pyrrolidine moiety, which enhances its reactivity and selectivity in various chemical reactions. It is particularly valuable in the development of pharmaceuticals, where it serves as a key intermediate in the synthesis of biologically active compounds. Researchers utilize this compound for its ability to form stable complexes with diols, making it an essential reagent in cross-coupling reactions and in the preparation of boron-containing compounds.

In addition to its synthetic utility, 4-[(1-Pyrrolidinyl)carbonyl]phenylboronic acid has shown promise in the field of cancer research, where it is being explored for its potential to inhibit specific enzymes involved in tumor progression. Its unique structural features allow for targeted modifications, enabling the design of novel therapeutic agents. With its broad range of applications and significant potential in drug discovery, this compound is an indispensable tool for researchers and industry professionals alike.

Synonyms
4-[(1-Pyrrolidinyl)carbonyl]benzeneboronic acid
CAS Number
389621-81-2
Purity
97 - 105% (Assay by titration)
Molecular Formula
C11H14BNO3
Molecular Weight
219.05
MDL Number
MFCD03411950
PubChem ID
2773571
Melting Point
136 - 140 °C
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-[(1-Pyrrolidinyl)carbonyl]benzeneboronic acid
CAS Number
389621-81-2
Purity
97 - 105% (Assay by titration)
Molecular Formula
C11H14BNO3
Molecular Weight
219.05
MDL Number
MFCD03411950
PubChem ID
2773571
Melting Point
136 - 140 °C
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-[(1-Pyrrolidinyl)carbonyl]phenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a crucial intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting cancer and diabetes.
  • Bioconjugation: It is employed in bioconjugation techniques to attach biomolecules to surfaces or other molecules, enhancing the efficacy of drug delivery systems.
  • Sensor Technology: The compound is used in the creation of sensors for detecting biomolecules, providing a sensitive and selective method for monitoring biological processes.
  • Organic Synthesis: It plays a significant role in organic synthesis, particularly in the formation of carbon-carbon bonds, which is essential for building complex organic structures.
  • Material Science: This chemical is utilized in the development of advanced materials, including polymers and nanomaterials, which have applications in electronics and nanotechnology.

Citations