N-(2-Bromoethyl)phthalimide

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CAS:574-98-1
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CAS:574-98-1
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CAS:574-98-1
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N-(2-Bromoethyl)phthalimide manufacturers

N-(2-Bromoethyl)phthalimide Basic information
Product Name:N-(2-Bromoethyl)phthalimide
Synonyms:AURORA KA-575;BETA-BROMOETHYLPHTHALIMIDE;TIMTEC-BB SBB003129;1-Bromo-2-phthalimidoethane;1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)-;2-(2-Bromoethyl)-1H-isoindole-1,3(2H)-dione;2-(2-bromoethyl)-1h-isoindole-3(2h)-dione;2-(2-Bromoethyl)phthalimide
CAS:574-98-1
MF:C10H8BrNO2
MW:254.08
EINECS:209-379-9
Product Categories:N-Substituted Maleimides, Succinimides & Phthalimides;N-Substituted Phthalimides;Bifunctional CrosslinkersOrganic Building Blocks;Carbonyl Compounds;Cyclic Imides;Linkers;Peptide Synthesis;Bifunctional Linkers;Building Blocks;Carbonyl Compounds;Chemical Biology;Chemical Synthesis;Cyclic Imides;Linkers and Crosslinkers;Organic Building Blocks;alkyl bromide
Mol File:574-98-1.mol
N-(2-Bromoethyl)phthalimide Structure
N-(2-Bromoethyl)phthalimide Chemical Properties
Melting point 80-83 °C (lit.)
Boiling point 318 °C
density 1.6254 (rough estimate)
refractive index 1.6320 (estimate)
storage temp. Sealed in dry,Room Temperature
form Crystalline Powder
pka-2.35±0.20(Predicted)
color White to slightly pink or beige
Water Solubility insoluble
BRN 148736
CAS DataBase Reference574-98-1(CAS DataBase Reference)
NIST Chemistry ReferenceN-(beta-bromoethyl)phthalimide(574-98-1)
EPA Substance Registry System1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)- (574-98-1)
Safety Information
Risk Statements 36/37/38
Safety Statements 24/25
WGK Germany 3
TSCA Yes
HS Code 29251995
MSDS Information
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N-(2-Bromoethyl)phthalimide Usage And Synthesis
Chemical Propertieswhite powder
UsesN-(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.
Synthesis Reference(s)Journal of the American Chemical Society, 71, p. 2425, 1949 DOI: 10.1021/ja01175a052
Organic Syntheses, Coll. Vol. 1, p. 119, 1941
Purification MethodsThe following is to be carried out in an efficient FUME HOOD. Dissolve the compound (180g) in CS2 (500 mL) by refluxing for 15minutes (to cause the separation of the most likely impurity, 1,2-diphthalimidoethane), filter and evaporate under reduced pressure. The product forms light tan crystals (m 78-80o). Recrystallise it from EtOH (charcoal) [the compound (50g) is dissolved in hot 75% EtOH (200mL), boiled for ca 10 minutes, carbon is added (5g, Norite), filter and cool to 0o], to give white crystals (40g) which can be recrystallised (m 80-81o); and further recrystallisation gives m 82-83o. [Salzberg & Supniewski Org Synth Coll Vol I 119 1932, Landini & Rolla Synthesis 389 1976, Beilstein 21/10 V 275.]
Tag:N-(2-Bromoethyl)phthalimide(574-98-1) Related Product Information
N-(3-BROMOPROPYL)PHTHALIMIDE N-Methylphthalimide Succinimide Bismaleimide Potassium phthalimide 4-Aminophthalimide 4-Nitrophthalimide 3-Nitrophthalimide N-Hydroxyphthalimide O-Phthalimide DIALIFOS Isoindoline BROMO 2-DEOXY-2-N-PHTHALIMIDO-3,4,6-TRI-O-ACETYL-A, B-D-GLUCOPYRANOSIDE (S)-N-(1-BROMO-2-PROPYL)PHTHALIMIDE N-(2-Bromoethyl)phthalimide 2-(2-bromoethyl)-5-nitro-2,3-dihydro-1H-isoindole-1,3-dione 2-(2-bromoethyl)-4-nitro-1H-isoindole-1,3(2H)-dione SPECS AJ-333/25116002