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CS-W001157 4
Total: USD 88.00

(3-Aminophenyl)boronic acid hydrochloride

  • CAS No. 85006-23-1

  • Cat. No. CS-W000982
  • Purity≥97%
  • MDL No.MFCD00191748

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

(3-Aminophenyl)boronic acid hydrochloride|CS-W000982

Structure of 85006-23-1

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General Information

  • CAS No. 85006-23-1
  • Cat. No. CS-W000982
  • Purity ≥97%
  • MDL No. MFCD00191748
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₉BClNO₂
  • Molecular Weight 173.41
  • Synonym(s) 3-Aminophenylboronicacid hydrochloride
  • SMILES OB(O)C1=CC=CC(N)=C1.Cl

Description

3-Aminophenylboronic acid hydrochloride is a boronic acid derivative that is commonly used as a reagent in Suzuki-Miyaura coupling reactions, where it can be used to form C-C bonds by the reaction with aryl or vinyl halides. It can also be used in other cross-coupling reactions, such as copper-catalyzed coupling reactions, as well as in palladium-free cross-coupling reactions.3-Aminophenylboronic acid hydrochloride was used as a key reagent used in the synthesis of the boronic acid ester starting material, which is subsequently converted to the cyclobutene precursor through a Heck coupling reaction. It is also used as a boronic acid source in the synthesis of boronate-functionalized monomers. These monomers are further used in the preparation of reproducible and high-quality polymer films.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H315-H319-H335
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501

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Computational Chemistry Data

  • TPSA   66.48
  • LogP   -0.6296
  • H_Acceptors   3
  • H_Donors   3
  • Rotatable_Bonds   1

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