ChemicalBook Product Catalog Chemical Reagents Organic reagents Imide N-Benzylmaleimide

N-Benzylmaleimide

N-Benzylmaleimide Basic information
Product Name:N-Benzylmaleimide
Synonyms:1H-Pyrrole-2,5-dione, 1-(phenylmethyl)-;ASISCHEM D48963;AKOS MSC-0016;AKOS 90883;eimide;(2S)-2-[[[4-[2-(2-amino-4-oxo-1H-pteridin-6-yl)ethylamino]cyclohexyl]-oxomethyl]amino]pentanedioic acid;1-BENZYL-PYRROLE-2,5-DIONE;1-BENZYL-1H-PYRROLE-2,5-DIONE
CAS:1631-26-1
MF:C11H9NO2
MW:187.19
EINECS:216-631-1
Product Categories:N-Substituted Maleimides;N-Substituted Maleimides, Succinimides & Phthalimides;Intermediates of Dyes and Pigments;PHARMACEUTICAL INTERMEDIATES;Heterocycles;Carbonyl Compounds;Cyclic Imides;Organic Building Blocks
Mol File:1631-26-1.mol
N-Benzylmaleimide Structure
N-Benzylmaleimide Chemical Properties
Melting point 70 °C (lit.)
Boiling point 177 °C / 20mmHg
density 1 g/cm3
storage temp. Inert atmosphere,Room Temperature
solubility Chloroform (Slightly), Methanol (Slightly)
form powder to crystal
pka-2.21±0.20(Predicted)
color White to Almost white
Water Solubility Insoluble
BRN 135801
CAS DataBase Reference1631-26-1(CAS DataBase Reference)
NIST Chemistry ReferenceN-benzylmaleimide(1631-26-1)
Safety Information
Hazard Codes C,T
Risk Statements 34-25-20/21
Safety Statements 26-36/37/39-45
RIDADR UN 1759 8/PG 2
WGK Germany 3
Hazard Note Irritant
HazardClass 8
PackingGroup III
HS Code 29251900
MSDS Information
ProviderLanguage
1-Benzyl-1H-pyrrole-2,5-dione English
ACROS English
SigmaAldrich English
ALFA English
N-Benzylmaleimide Usage And Synthesis
Chemical Propertiesoff-white to light yellow
UsesN-Benzylmaleimide is used as plastic additive, Pharmaceutical Intermediates. It is an important raw material intermediate used in organic Synthesis, Pharmaceuticals, Agrochemicals Dyestuff.
General DescriptionN-Benzylmaleimide is an N-substituted maleimide and its microwave-mediated facile and fast synthesis has been described. Radical and anionic copolymerization of N-benzylmaleimide with optically active N-(L-menthoxycarbonylmethyl)maleimide has been reported. Base-catalyzed asymmetric cycloaddition of anthrone with N-benzylmaleimide was studied in the presence of C2-chiral pyrrolidines. Stereoselctive iridium-catalyzed double incorporation reaction of styrene with N-benzylmaleimide affords cyclic product.
N-Benzylmaleimide Preparation Products And Raw materials
Preparation Products5-NITROFURFURYL ALCOHOL
N-Phenylmaleimide 1-[(2-methoxyphenyl)methyl]-2,5-dihydro-1H-pyrrole-2,5-dione O-Phthalimide (S)-N-(1-(1-NAPHTHYL) ETHYL)MALEIMIDE Benzyl chloride Bismaleimide (S)-(-)-N-(1-PHENYLETHYL)MALEIMIDE Benzyl alcohol Pyrrole Succinimide DIALIFOS N-Ethylmaleimide Maleimide Benzyl 1-(1-phenylethyl)-2,5-dihydro-1H-pyrrole-2,5-dione Benzyl benzoate Benzyl nicotinate N-Benzylmaleimide
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