Substance

ID:318555

3,3-Dimethyl-1-(trifluoromethyl)-1,2-benziodoxole

Names and Identifiers
IUPAC Traditional name
3,3-dimethyl-1-(trifluoromethyl)-1λ3,2-benziodaoxole
IUPAC name
3,3-dimethyl-1-(trifluoromethyl)-3H-1λ3,2-benziodaoxole
Synonyms
1,3-Dihydro-3,3-dimethyl-1-(trifluoromethyl)-1,2-benziodoxole1,3-二氢-3,3-二甲基-1-(三氟甲基)-1,2-苯并碘氧杂戊环3,3-Dimethyl-1-(trifluoromethyl)-1,2-benziodoxoleTogni’s ReagentTogni 试剂3,3-二甲基-1-(三氟甲基)-1,2-苯并碘氧杂戊环
Registration numbers
CAS Number
MDL Number
Properties
Safety Information
GHS Signal Word
Warning
Risk Statements
36/37/38
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
GHS Pictograms
GHS07
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
German water hazard class
3
Safety Statements
26-36/37
European Hazard Symbols
Irritant Irritant (Xi)
MSDS Link
GHS Precautionary statements
P261-P305+P351+P338
GHS Hazard statements
H315-H319-H335
Storage Temperature
2-8°C
Product Information
Empirical Formula (Hill Notation)
C10H10F3IO
Purity
95%
Physical Property
Melting Point
75-79 °C
Molecule Details
Packaging
1, 5 g in glass bottle
250 mg in glass bottle
Application
Easily accessible hypervalent iodine compound acting as an electrophilic CF3-transfer reagent for direct, mild, and efficient trifluoromethylation.1 Trifluoromethylation of a variety of compounds including:
• Secondary and primary aryl- and alkylphospines1
• Phenols2
• Peptides containing cysteine residudes by SPPS and electrophilic S-trifluoromethylation3
• Arenes and N-heterocycles4
• Electrophilic N-trifluoromethylation of Arozoles5
Molecular Spectra
No Data Available
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References
No Data Available
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