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N-(Phenylseleno)phthalimide_Molecular_structure_CAS_71098-88-9)
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N-(Phenylseleno)phthalimide

Catalog No. B21125 Name Alfa Aesar
CAS Number 71098-88-9 Website
M. F. C14H9NO2Se Telephone
M. W. 302.18676 Fax
Purity tech. 85% Email
Storage Chembase ID: 145763

SYNONYMS

Title
N-(苯硒基)邻苯二甲酰亚胺
IUPAC name
2-(phenylselanyl)-2,3-dihydro-1H-isoindole-1,3-dione
IUPAC Traditional name
2-(phenylselanyl)isoindole-1,3-dione

DATABASE IDS

Beilstein Number 1468701
MDL Number MFCD00010406
CAS Number 71098-88-9

PROPERTIES

Purity tech. 85%
Melting Point ca 180°C
GHS Pictograms GHS06
GHS Pictograms GHS08
GHS Pictograms GHS09
GHS Hazard statements H301-H331-H373-H400-H410
European Hazard Symbols Toxic Toxic (T)
European Hazard Symbols Nature polluting Nature polluting (N)
GHS Precautionary statements P260-P261-P301+P310-P321-P405-P501A
Risk Statements 23/25-33-50/53
Safety Statements 20/21-28-45-60-61
Storage Warning Moisture Sensitive
TSCA Listed
Hazard Class 6.1
UN Number UN3283
Packing Group II

DETAILS

REFERENCES

  • Reagent for the oxy-selenation of alkenes in the presence of 2-3 equivalents of water and an acid catalyst: J. Am. Chem. Soc., 101, 3704 (1979). The trans-?-hydroxy selenide products are useful intermediates, e.g. in the synthesis of allylic alcohols by selenoxide elimination. In general, the reagent is superior to the corresponding halides in intramolecular cyclization reactions with unsaturated acids, urethanes, etc. Even suitably disposed ketones may undergo cyclization of the enol form, in the presence of SnCl4: J. Chem. Soc., Chem. Commun., 1251, 1252 (1982):