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101251-09-6

101251-09-6 Structure

101251-09-6 Structure
IdentificationMore
[Name]

4-Acetamidophenylboronic acid
[CAS]

101251-09-6
[Synonyms]

4-ACETAMIDBENZENEBORONIC ACID
4-ACETAMIDOBENZENEBORONIC ACID
4-ACETAMIDOPHENYLBORONIC ACID
4-ACETAMINOPHENYLBORONIC ACID
4-ACETYLAMINOPHENYLBORONIC ACID
P-ACETAMIDOPHENYLBORONIC ACID
TIMTEC-BB SBB000202
4-Acetamidophenylboronic acid, 97+%
[Molecular Formula]

C8H10BNO3
[MDL Number]

MFCD02179451
[Molecular Weight]

178.98
[MOL File]

101251-09-6.mol
Chemical PropertiesBack Directory
[Appearance]

White to light yellow crystal powde
[Melting point ]

215-220 °C (lit.)
[density ]

1.23±0.1 g/cm3(Predicted)
[storage temp. ]

Refrigerator (+4°C)
[form ]

Powder
[pka]

8.63±0.10(Predicted)
[color ]

Gray-tan
[Water Solubility ]

85 g/L (70 ºC)
[InChI]

1S/C8H10BNO3/c1-6(11)10-8-4-2-7(3-5-8)9(12)13/h2-5,12-13H,1H3,(H,10,11)
[InChIKey]

VYEWTHXZHHATTA-UHFFFAOYSA-N
[SMILES]

CC(=O)Nc1ccc(cc1)B(O)O
[CAS DataBase Reference]

101251-09-6(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Safety Statements ]

S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HS Code ]

29319090
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Chemical Properties]

White to light yellow crystal powde
[Uses]

Reactant involved in:
  • Synthesis of TpI2 kinase inhibitors
  • Biological evaluation of modulators of survival motor neuron protein
  • Cross-coupling with conjugated dienes or terminal alkenes or diazoesters
  • Synthesis of tetrabutylammonium trifluoroborates
  • Rhosium-catalyzed cyanation
[Synthesis]

4-Aminophenylboronic acid

89415-43-0

Acetyl chloride

75-36-5

4-Acetamidophenylboronic acid

101251-09-6

To a three-neck flask was added 13.7 g (0.1 mol) of 4-aminophenylboronic acid and 100 mL of trichloromethane. After thorough stirring, the reaction mixture was cooled to 5 °C and then 23.4 g (0.3 mol) of acetyl chloride was added slowly dropwise. After maintaining the reaction temperature at 5°C to complete the dropwise addition, the reaction system was warmed to 40°C and the reaction continued to be stirred for 3 hours. Upon completion of the reaction, 150 mL of water was added to the reaction mixture and the resulting solid product was washed with stirring. Subsequently, the solid was separated by filtration and washed with an appropriate amount of cold water. Finally, the resulting solid was dried in a vacuum drying oven to obtain 14 g of white or off-white solid powder 4-acetylaminophenylboronic acid in 78.2% yield.

[References]

[1] Patent: CN106946920, 2017, A. Location in patent: Paragraph 0017; 0018; 0020
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

4-Acetamidophenylboronic acid, 97+%(101251-09-6)
[Sigma Aldrich]

101251-09-6(sigmaaldrich)
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