Substance
ID:317320
Names and Identifiers
IUPAC name
(quinolin-3-yl)boronic acid
IUPAC Traditional name
quinolin-3-ylboronic acid
Synonyms
3-Quinolineboronic acid3-喹啉硼酸(3-Quinolinyl)boronic acid(3-Quinolyl)boronic acidQuinolin-3-ylboronic acid
Properties
Safety Information
Safety Statements
26-36-37
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
GHS Signal Word
Warning
GHS Precautionary statements
P261-P305+P351+P338
European Hazard Symbols
Irritant (Xi)German water hazard class
3
GHS Hazard statements
H315-H319-H335
MSDS Link
Risk Statements
36/37/38
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Storage Temperature
2-8°C
Product Information
Grade
technical grade
Empirical Formula (Hill Notation)
C9H8BNO2
Physical Property
Melting Point
191-196 °C
Molecule Details
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
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
Molecular Spectra
No Data Available
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References
No Data Available
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