Weight | 142.118 g/mol |
---|---|
Formula | C4H6N4O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 4 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
Glycoluril (496-46-8)
acetyleneurea · tetrahydroimidazo(4,5-d)imidazole-2,5(1H,3H)-dione · perhydroimidazo(4,5-d)imidazole-2,5-dione
Score:
#5739 in Chemistry
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- Iodination of proteins, glycoproteins, and peptides using a solid-phase oxidizing agent, 1,3,4,6-tetrachloro-3,6-diphenyl glycoluril (Iodogen) (Analytical Biochemistry, 1981)
- I. Ueber Condensationsproducte aus Glycoluril und Formaldehyd (European Journal of Organic Chemistry, 1905)
- Molecular and Supramolecular Objects from Glycoluril (Accounts of Chemical Research, 1999)
- Templated synthesis of glycoluril hexamer and monofunctionalized cucurbit[6]uril derivatives. (Journal of the American Chemical Society, 2011)
- Ruthenium(II) complexes of bipyridine-glycoluril and their interactions with DNA. (Bioconjugate Chemistry, 2009)
- Methylene-Bridged Glycoluril Dimers: Synthetic Methods (Journal of Organic Chemistry, 2002)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - acetyleneurea
- tetrahydroimidazo(4,5-d)imidazole-2,5(1H,3H)-dione
- perhydroimidazo(4,5-d)imidazole-2,5-dione
-
SMILESC12C(NC(=O)N1)NC(=O)N2
-
InChIKeyVPVSTMAPERLKKM-UHFFFAOYSA-N
- Pubchem - Glycoluril
- Wikipedia - glycoluril
Glycoluril is an organic chemical composed of two cyclic urea groups joined across the same two-carbon chain. It is a white powder that has been used in water treatment, in paints and coatings, and occasionally as a slow-release fertilizer, and also occurs as the most prevalent impurity in commercial allantoin supplies. Glycouril itself and derivatives of it are used as monomers for producing the macrocyclic cucurbiturils polymers, which serve as hosts to bind to various neutral and anionic species.
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