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Home Other Building Blocks 1-Hydroxy-1H-pyrrole-2,5-dione

1-Hydroxy-1H-pyrrole-2,5-dione

CAS No.:
4814-74-8
Catalog Number:
AG003EF1
Molecular Formula:
C4H3NO3
Molecular Weight:
113.0715
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Product Description
Catalog Number:
AG003EF1
Chemical Name:
1-Hydroxy-1H-pyrrole-2,5-dione
CAS Number:
4814-74-8
Molecular Formula:
C4H3NO3
Molecular Weight:
113.0715
MDL Number:
MFCD00005501
IUPAC Name:
1-hydroxypyrrole-2,5-dione
InChI:
InChI=1S/C4H3NO3/c6-3-1-2-4(7)5(3)8/h1-2,8H
InChI Key:
BUXKULRFRATXSI-UHFFFAOYSA-N
SMILES:
ON1C(=O)C=CC1=O
EC Number:
225-385-4
Properties
Complexity:
154  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
113.011g/mol
Formal Charge:
0
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
113.072g/mol
Monoisotopic Mass:
113.011g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
57.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-1  
Literature
Title Journal
One-electron oxidation of ferrocenes by short-lived N-oxyl radicals. The role of structural effects on the intrinsic electron transfer reactivities. Organic & biomolecular chemistry 20110607
N-hydroxyimides as efficient ligands for the copper-catalyzed N-arylation of pyrrole, imidazole, and indole. The Journal of organic chemistry 20071109
Coupling of contact sensitizers to thiol groups is a key event for the activation of monocytes and monocyte-derived dendritic cells. The Journal of investigative dermatology 20030201
Cyclization strategies for the synthesis of macrocyclic bisindolylmaleimides. The Journal of organic chemistry 20010323
Properties