1H-Pyrrole-2,5-dione, 3,4-dibromo-1-(phenylmethyl)-


Chemical Name: 1H-Pyrrole-2,5-dione, 3,4-dibromo-1-(phenylmethyl)-
CAS Number: 91026-00-5
Product Number: AG0035C8(AGN-PC-0KUQAF)
Synonyms:
MDL No:
Molecular Formula: C11H7Br2NO2
Molecular Weight: 344.9868

Identification/Properties


Properties
Form:
Solid
Computed Properties
Molecular Weight:
344.99g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
344.882g/mol
Monoisotopic Mass:
342.884g/mol
Topological Polar Surface Area:
37.4A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
335
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

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Chemical Structure



N-Benzyl-2,3-dibromomaleimide is a versatile compound widely used in chemical synthesis. Its key application lies in its ability to serve as an efficient and selective dienophile in Diels-Alder reactions. This compound participates in cycloaddition reactions with dienes to form fused cyclic compounds with high regio- and stereo-selectivity. Additionally, N-Benzyl-2,3-dibromomaleimide can undergo nucleophilic substitution reactions, making it a valuable building block for the synthesis of various heterocyclic compounds. Its unique properties and reactivity make it a valuable tool for the efficient construction of complex molecules in organic synthesis.