2-Aminophenylboronic acid pinacol ester

• Catalog No.: 576557
• CAS Number: 191171-55-8
• M. F.: C12H18BNO2
• M. W.: 219.08782

SYNONYMS

• Title: 2-氨基苯硼酸频哪醇酯
• IUPAC name: 2-(tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
• IUPAC Traditional name: 2-(tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
• Synonyms: 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline; 2-(4,4,5,5-四甲基-1,3,2-二氧杂环戊硼烷-2-基)苯胺

DATABASE IDS

• MDL Number: MFCD02179448
• PubChem SID: 24880867
• CAS Number: 191171-55-8

PROPERTIES

• Empirical Formula (Hill Notation): C12H18BNO2
• Melting Point: 63-68 °C(lit.)
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• GHS Precautionary statements: P261-P305 + P351 + P338
• Risk Statements: 36/37/38
• Safety Statements: 26-36
• German water hazard class: 3

DETAILS

Description (English)

Packaging
1, 5 g in glass bottle
Application
Reactant involved in synthesis of:
• Indolo[3,4-cd][1]benzazepines via Pictet-Spengler-type cyclizations1
• Antimicrobial amphiphilic aryl peptideomimetics2
• Pyridoquinazolines and benzo[h][1,6]naphthyridines via intramolecular electrophilic substitution reactions3
• Thienopyridine derivatives4
• Dihydroquinolones5
• Methacrylamidophenylboronic acids6

Description (简体中文)

包装
1, 5 g in glass bottle
Application
Reactant involved in synthesis of:
• Indolo[3,4-cd][1]benzazepines via Pictet-Spengler-type cyclizations1
• Antimicrobial amphiphilic aryl peptideomimetics2
• Pyridoquinazolines and benzo[h][1,6]naphthyridines via intramolecular electrophilic substitution reactions3
• Thienopyridine derivatives4
• Dihydroquinolones5
• Methacrylamidophenylboronic acids6