Substance
ID:318484
Names and Identifiers
IUPAC Traditional name
2-chloro-5-(trifluoromethyl)phenylboronic acid
IUPAC name
[2-chloro-5-(trifluoromethyl)phenyl]boronic acid
Synonyms
2-氯-5-(三氟甲基)苯硼酸2-Chloro-5-(trifluoromethyl)benzeneboronic acid2-Chloro-5-(trifluoromethyl)phenylboronic acid
Properties
Safety Information
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
GHS Signal Word
Warning
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
European Hazard Symbols
Irritant (Xi)GHS Hazard statements
H315-H319-H335
German water hazard class
3
Safety Statements
26
MSDS Link
GHS Precautionary statements
P261-P305+P351+P338
Risk Statements
36/37/38
Product Information
Empirical Formula (Hill Notation)
C7H5BClF3O2
Molecule Details
Application
May contain varying amounts of anhydride.
Reactant for:
• Synthesis of aryl- and hetarylfurocoumarins via Suzuki reaction1
• Synthesis of Et canthinone-3-carboxylates from Et 4-bromo-6-methoxy-1,5-naphthyridine-3-carboxylate via a Pd-catalyzed Suzuki-Miyaura coupling and a Cu-catalyzed amidation reaction2
• Preparation of xanthines via one-pot coupling with diaminouracil3
• Pd-catalyzed Suzuki-Miyaura coupling with 8-bromo-1,5-naphthyridin-2-one4
Packaging
1, 10 g in glass bottle
May contain varying amounts of anhydride.
Reactant for:
• Synthesis of aryl- and hetarylfurocoumarins via Suzuki reaction1
• Synthesis of Et canthinone-3-carboxylates from Et 4-bromo-6-methoxy-1,5-naphthyridine-3-carboxylate via a Pd-catalyzed Suzuki-Miyaura coupling and a Cu-catalyzed amidation reaction2
• Preparation of xanthines via one-pot coupling with diaminouracil3
• Pd-catalyzed Suzuki-Miyaura coupling with 8-bromo-1,5-naphthyridin-2-one4
Packaging
1, 10 g in glass bottle
Molecular Spectra
No Data Available
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References
No Data Available
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