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N-(2-Bromoethyl)phthalimide, 97+%, Thermo Scientific Chemicals
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Catalog number A12164.22
also known as A12164-22
Price (USD)/ Each
120.00
-
Quantity:
100 g
Price (USD)/ Each
120.00
N-(2-Bromoethyl)phthalimide, 97+%, Thermo Scientific Chemicals
Catalog numberA12164.22
Price (USD)/ Each
120.00
-
Chemical Identifiers
CAS574-98-1
IUPAC Name2-(2-bromoethyl)-2,3-dihydro-1H-isoindole-1,3-dione
Molecular FormulaC10H8BrNO2
InChI KeyCHZXTOCAICMPQR-UHFFFAOYSA-N
SMILESBrCCN1C(=O)C2=CC=CC=C2C1=O
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White to cream
FormCrystals or powder or crystalline powder
Identification (FTIR)Conforms
Melting Point (clear melt)80.0-87.0°C
Assay (GC)≥97.0%
N-(2-Bromoethyl)phthalimide is an intermediate used in organic synthesis. It can react with phenyl magnesium bromide to get 2-(2-bromo-ethyl)-3-hydroxy-3-phenyl-isoindolin-1-one.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
N-(2-Bromoethyl)phthalimide is an intermediate used in organic synthesis. It can react with phenyl magnesium bromide to get 2-(2-bromo-ethyl)-3-hydroxy-3-phenyl-isoindolin-1-one.
Solubility
Soluble in water (224 mg/L at 25°C).
Notes
Store in cool, dry place in a tightly sealed container. Store away from oxidizing agent.
N-(2-Bromoethyl)phthalimide is an intermediate used in organic synthesis. It can react with phenyl magnesium bromide to get 2-(2-bromo-ethyl)-3-hydroxy-3-phenyl-isoindolin-1-one.
Solubility
Soluble in water (224 mg/L at 25°C).
Notes
Store in cool, dry place in a tightly sealed container. Store away from oxidizing agent.
RUO – Research Use Only
General References:
- T. Karthick; V. Balachandranb; S. Perumal; A. Nataraj. Rotational isomers, vibrational assignments, HOMO-LUMO, NLO properties and molecular electrostatic potential surface of N-(2 bromoethyl) phthalimide. Journal of Molecular Structure. 2011, 1005 (1-3), 202-213.
- De Kimpe N.; Virag M.; Keppens M.; Scheinmann F.; Stachulski A.V. Cyclocondensation Of N-(2-Bromoethyl)Phthalimide With The Dianon Of Isobutyric Acid To A Functionalized 2,3- Dihydrooxazolo2,3-Aisoindol-5(9Bh)-One De Rivative. J. Chem. Res., Synop. 1995, 6, 252-253.