3-Quinolineboronic acid

• Catalog No.: 691909
• CAS Number: 191162-39-7
• M. F.: C9H8BNO2
• M. W.: 172.97632

SYNONYMS

• Title: 3-喹啉硼酸
• IUPAC name: (quinolin-3-yl)boronic acid
• IUPAC Traditional name: quinolin-3-ylboronic acid
• Synonyms: (3-Quinolyl)boronic acid; (3-Quinolinyl)boronic acid; Quinolin-3-ylboronic acid

DATABASE IDS

• MDL Number: MFCD02183527
• CAS Number: 191162-39-7

PROPERTIES

• Empirical Formula (Hill Notation): C9H8BNO2
• Grade: technical grade
• Melting Point: 191-196 °C
• 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: 26-36-37
• Storage Temperature: 2-8°C
• German water hazard class: 3

DETAILS

Description (English)

Application
May contain varying amounts of anhydride.
Reactant for:
• Preparation of P1-substituted symmetry-based human immunodeficiency virus protease inhibitors with antiviral activity against drug-resistant viruses1
• Preparation of heterobiaryls via Suzuki-Miyaura cross-coupling with heteroaryl halides in continuous flow2
• Preparation of Ph and heterocyclic(pyridinyl)pyrazolyl)pyridines as TGF-1 and activin A signalling inhibitors3
• Copper-mediated trifluoromethylation4
• Synthesis and bioactivity of combretastatin analogs via regioselective Suzuki coupling of dihaloheteroaromatic compounds5
• Suzuki-Miyaura cross-coupling reactions6
Packaging
1, 5 g in glass bottle

Description (简体中文)

Application
可能含不定量的酸酐。
Reactant for:
• Preparation of P1-substituted symmetry-based human immunodeficiency virus protease inhibitors with antiviral activity against drug-resistant viruses1
• Preparation of heterobiaryls via Suzuki-Miyaura cross-coupling with heteroaryl halides in continuous flow2
• Preparation of Ph and heterocyclic(pyridinyl)pyrazolyl)pyridines as TGF-1 and activin A signalling inhibitors3
• Copper-mediated trifluoromethylation4
• Synthesis and bioactivity of combretastatin analogs via regioselective Suzuki coupling of dihaloheteroaromatic compounds5
• Suzuki-Miyaura cross-coupling reactions6
包装
1, 5 g in glass bottle