2-Aminophenylboronic acid pinacol ester

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
EINECS:
Product Categories:Boronic Acid;Boronic acids;Amines;blocks;BoronicAcids;Substituted Boronic Acids
Mol File:191171-55-8.mol
2-Aminophenylboronic acid pinacol ester Structure
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)
pka3.51±0.10(Predicted)
form Crystalline Powder
color Cream
Water Solubility Insoluble
Sensitive Air Sensitive
BRN 8548809
CAS DataBase Reference191171-55-8(CAS DataBase Reference)
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 Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
2-Aminophenylboronic acid pinacol ester Usage And Synthesis
Chemical Propertiescream crystalline powder
UsesReactant 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
UsesReactant 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
Reactions2-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 ester Preparation Products And Raw materials
Preparation Products2-Aminophenylboronic acid
4-Aminophenylboronic acid 2-AMINO-4-METHYLPHENYLBORONIC ACID, PINACOL ESTER Benzocaine Sulfanilic acid 2-AMINO-5-CHLOROPHENYLBORONIC ACID, PINACOL ESTER 2-Morpholin-4-yl-5-(trifluoromethyl)benzeneboronic acid, pinacol ester 2-BORONOBENZALDEHYDE, PINACOL ESTER Tris(trimethylsilyl)phosphate 2-Acetylaminophenylboronic acid pinacol ester (2-Amino-4-methoxycarbonylphenyl)boronic acid pinacol ester hydrochloride Acid Blue 93 Sulfanilamide Aniline (2-BOC-AMINOPHENYL)BORONIC ACID, PINACOL ESTER 2-Aminophenylboronic acid pinacol ester 2-(4-TERT-BUTOXYCARBONYLPIPERAZINYL)PHENYLBORONIC ACID, PINACOL ESTER DIMETHYL[2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL]AMINE 2-(MORPHOLINO)PHENYLBORONIC ACID PINACOLATE

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