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Catalog Number:
40005
CAS Number:
616880-14-9
N- [4-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)phényl]méthanesulfonamide
Purity:
≥ 97% (CG)
Synonym(s):
Ester pinacol de l'acide 4-(méthanesulfonylamino)phénylboronique, 2-[4-(méthanesulfonylamino)phényl]-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
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Product Information

N-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanesulfonamide is a versatile compound that plays a significant role in various fields, particularly in medicinal chemistry and material science. This compound is recognized for its unique boron-containing structure, which enhances its reactivity and stability, making it an excellent candidate for applications in drug development and synthesis. Its sulfonamide group contributes to its solubility and bioactivity, facilitating its use in pharmaceutical formulations. Researchers have utilized this compound in the development of targeted therapies, where its ability to form stable complexes with biological targets is particularly advantageous.

In addition to its pharmaceutical applications, N-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanesulfonamide is also valuable in organic synthesis, where it serves as a building block for more complex molecules. Its distinctive properties allow for the creation of innovative materials with enhanced performance characteristics. This compound stands out in its class due to its dual functionality, combining the benefits of boron chemistry with sulfonamide reactivity, making it a preferred choice for researchers and industry professionals seeking efficient and effective solutions in their projects.

Synonyms
Ester pinacol de l'acide 4-(méthanesulfonylamino)phénylboronique, 2-[4-(méthanesulfonylamino)phényl]-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
CAS Number
616880-14-9
Purity
≥ 97% (CG)
Molecular Formula
C 13 H 20 BNO 4 S
Molecular Weight
297.18
MDL Number
MFCD05663876
PubChem ID
16217653
Melting Point
195 - 199 °C
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Ester pinacol de l'acide 4-(méthanesulfonylamino)phénylboronique, 2-[4-(méthanesulfonylamino)phényl]-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
CAS Number
616880-14-9
Purity
≥ 97% (CG)
Molecular Formula
C 13 H 20 BNO 4 S
Molecular Weight
297.18
MDL Number
MFCD05663876
PubChem ID
16217653
Melting Point
195 - 199 °C
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

N-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanesulfonamide is widely utilized in research focused on:

  • Drug Development: This compound serves as a crucial intermediate in the synthesis of pharmaceuticals, particularly in developing targeted therapies for various diseases, enhancing efficacy and reducing side effects.
  • Bioconjugation: It is employed in bioconjugation processes, allowing researchers to attach biomolecules to drugs or imaging agents, improving delivery and specificity in therapeutic applications.
  • Material Science: The compound is used in the development of advanced materials, such as polymers and coatings, which exhibit improved thermal stability and mechanical properties, beneficial for various industrial applications.
  • Analytical Chemistry: It acts as a reagent in analytical methods, facilitating the detection and quantification of specific compounds in complex mixtures, thus aiding in quality control and research analysis.
  • Environmental Science: The compound is explored for its potential in environmental applications, such as the detection and remediation of pollutants, contributing to sustainability efforts in chemical management.

Citations