1-Benzylpyrrole-2,5-dione
1-Benzylpyrrole-2,5-dione structure
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Common Name | 1-Benzylpyrrole-2,5-dione | ||
|---|---|---|---|---|
| CAS Number | 1631-26-1 | Molecular Weight | 187.19 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 338.8±21.0 °C at 760 mmHg | |
| Molecular Formula | C11H9NO2 | Melting Point | 70 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 157.9±14.4 °C | |
| Symbol |
GHS05 |
Signal Word | Danger | |
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Construction of a single-chain Fv from an antibody which catalyses a Diels Alder cycloaddition.
Biochem. Soc. Trans. 24(2) , 313S, (1996)
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Parallel synthesis and purification using anthracene-tagged substrates.
Org. Lett. 2(22) , 3509-12, (2000) [reaction: see text] A new strategy for the synthesis and purification of synthetic intermediates is described using anthracene-tagged ester substrates in conjunction with an N-benzylmaleimide resin. Anthracene chemical tags permit use of standard solution-ph... |
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Copolymerization of optically active N-(l-menthoxycarbonylmethyl) maleimide with N-phenyl-or N-benzylmaleimide. Kagawa K, et al.
Polymer 36(5) , 941-48, (1995)
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Microwave-induced One-pot Synthesis of N-carboxyalkyl Maleimides and Phthalimides. Borah N, et al.
J. Chem. Res. Synop. 5 , 272-3, (1998)
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Asymmetric cycloaddition of anthrone with N-substituted maleimides with C2-chiral pyrrolidines. Tokioka K, et al.
Tetrahedron Asymmetry 8(1) , 101-7, (1997)
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Iridium-catalyzed double incorporation reaction of N-benzylmaleimide to styrene via ortho-C-H bond activation, initiated by precoordination of the double bond of styrene to iridium. Kiyooka S-I and Takeshita Y.
Tetrahedron Lett. 46(25) , 4279-82, (2005)
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