Substance
ID:326715
Names and Identifiers
IUPAC name
N-(5-chloropyridin-2-yl)-1,1,1-trifluoro-N-trifluoromethanesulfonylmethanesulfonamide
IUPAC Traditional name
N-(5-chloropyridin-2-yl)-1,1,1-trifluoro-N-trifluoromethanesulfonylmethanesulfonamide
Synonyms
N-(5-氯-2-吡啶基)双(三氟甲烷磺酰亚胺)2-[N,N-双(三氟甲基磺酰)氨基]-5-氯吡啶N,N-双(三氟甲基磺酰)-5-氯-2-吡啶胺Comins 试剂2-[N,N-Bis(trifluoromethylsulfonyl)amino]-5-chloropyridineN-(5-Chloro-2-pyridyl)bis(trifluoromethanesulfonimide)N,N-Bis(trifluoromethylsulfonyl)-5-chloro-2-pyridylamineComins’ Reagent
Registration numbers
MDL Number
Beilstein Number
CAS Number
PubChem SID
Properties
Safety Information
GHS Precautionary statements
P261-P305+P351+P338
GHS Signal Word
Warning
Storage Temperature
2-8°C
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
GHS Hazard statements
H315-H319-H335
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
German water hazard class
3
Safety Statements
26-36
European Hazard Symbols
Irritant (Xi)Physical Property
Melting Point
45-47 °C(lit.)
Product Information
Empirical Formula (Hill Notation)
C7H3ClF6N2O4S2
Purity
96%
Molecule Details
Packaging
1, 5 g in glass bottle
Application
Provides good yields of vinyl triflates from the corresponding ketone enolates or dienolates.1,2,3
Reactant for: Suzuki-Miyaura cross coupling Synthesis of nicotinic acetylcholine receptor-selective ligands Enantioselective desymmetrizing palladium catalyzed carbonylation reactions Synthesis of high affinity niacin receptor GPR109A agonists Preparation of heteroaromatics
1, 5 g in glass bottle
Application
Provides good yields of vinyl triflates from the corresponding ketone enolates or dienolates.1,2,3
Reactant for: Suzuki-Miyaura cross coupling Synthesis of nicotinic acetylcholine receptor-selective ligands Enantioselective desymmetrizing palladium catalyzed carbonylation reactions Synthesis of high affinity niacin receptor GPR109A agonists Preparation of heteroaromatics
Molecular Spectra
No Data Available
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References
No Data Available
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