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2-Aminophenylboronic acid pinacol ester

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2-Aminophenylboronic acid pinacol ester Basic information

Product Name:
2-Aminophenylboronic acid pinacol ester
Synonyms:
  • 2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)ANILINE
  • 2-AMINOPHENYLBORONIC ACID, PINACOL CYCLIC ESTER
  • 2-AMINOPHENYLBORONIC ACID, PINACOL ESTER
  • 2-AMINOBENZENEBORONIC ACID PINACOL ESTER
  • 2-Aminobenzeneboronic acid pinacol cyclic ester
  • -1,3,2-dioxaboroL
  • 2-(4,4,5,5-TetramethyL
  • an-2-yL
CAS:
191171-55-8
MF:
C12H18BNO2
MW:
219.09
Product Categories:
  • Boronic Acid
  • Boronic acids
  • Amines
  • blocks
  • BoronicAcids
  • Substituted Boronic Acids
  • OLED
Mol File:
191171-55-8.mol
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2-Aminophenylboronic acid pinacol ester Chemical Properties

Melting point:
63-68 °C (lit.)
Boiling point:
125°C/1.5mmHg(lit.)
Density 
1.05±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Methanol (Slightly)
pka
3.51±0.10(Predicted)
form 
Crystalline Powder
color 
Cream
Water Solubility 
Insoluble
Sensitive 
Air Sensitive
BRN 
8548809
CAS DataBase Reference
191171-55-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-20/21/22
Safety Statements 
26-36
WGK Germany 
3
HS Code 
29310099

MSDS

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2-Aminophenylboronic acid pinacol ester Usage And Synthesis

Chemical Properties

cream crystalline powder

Uses

Reactant involved in synthesis of:

  • Indolo[3,4-cd][1]benzazepines via Pictet-Spengler-type cyclizations
  • Antimicrobial amphiphilic aryl peptideomimetics
  • Pyridoquinazolines and benzo[h][1,6]naphthyridines via intramolecular electrophilic substitution reactions
  • Thienopyridine derivatives
  • Dihydroquinolones
  • Methacrylamidophenylboronic acids

Uses

Reactant involved in synthesis of: Indolo[3,4-cd]benzazepines via Pictet-Spengler-type cyclizations Antimicrobial amphiphilic aryl peptideomimetics Pyridoquinazolines and benzo[h] naphthyridines via intramolecular electrophilic substitution reaction

Reactions

2-Aminophenylboronic acid pinacol ester is a reactant involved in synthesis of:
??Indolo[3,4-cd] benzazepines via Pictet-Spengler-type cyclizations
??Antimicrobial amphiphilic aryl peptideomimetics
??Pyridoquinazolines and benzo[h]naphthyridines via intramolecular electrophilic substitution reactions
??Thienopyridine derivatives
??Dihydroquinolones
??Methacrylamidophenylboronic acids

2-Aminophenylboronic acid pinacol esterSupplier

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