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CS-W001157 4
Total: USD 88.00

(2-(Methylsulfonamido)phenyl)boronic acid

  • CAS No. 756520-78-2

  • Cat. No. CS-W014911
  • Purity≥96%
  • MDL No.MFCD02179471

*For research and further manufacturing use only, not for direct human use.

(2-(Methylsulfonamido)phenyl)boronic acid|CS-W014911

Structure of 756520-78-2

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General Information

  • CAS No. 756520-78-2
  • Cat. No. CS-W014911
  • Purity ≥96%
  • MDL No. MFCD02179471
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₁₀BNO₄S
  • Molecular Weight 215.03
  • Synonym(s) boronic acid, B-[2-[(methylsulfonyl)amino]phenyl]-
  • SMILES O=S(NC1=CC=CC=C1B(O)O)(C)=O

Description

This boronic acid features a methylsulfonamido group at the ortho position, enhancing solubility and metabolic stability. The pendant boronic acid moiety enables efficient Suzuki-Miyaura cross-coupling under standard conditions, facilitating rapid access to biaryl architectures in medicinal chemistry and materials synthesis.

Application

(2-(Methylsulfonamido)phenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. Its stability, ease of handling, and compatibility with diverse functional groups make it well-suited for constructing biaryl scaffolds in medicinal chemistry and materials science applications.

Synthesis

  • Route1
    • In-stock
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      5570-18-3
    • null|null
      124-63-0
    • ~16%
    • In-stock
      (2-(Methylsulfonamido)phenyl)boronic acid|CS-W014911
      756520-78-2

    References

    • Gavai, Ashvinikumar V.; Norris, Derek J.; Han, Wen-Ching; Vite, Gregory D.; Fink, Brian E.; Tokarski, John S. Patent: US2005/192310 A1, 2005 ; Location in patent: Page/Page column 47 ;

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302
Precautionary Statements : P264-P270-P330-P501

Quality Control

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Computational Chemistry Data

  • TPSA   86.63
  • LogP   -1.2621
  • H_Acceptors   4
  • H_Donors   3
  • Rotatable_Bonds   3

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