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Merck

G7305

Sigma-Aldrich

Glycoluril

97%

Synonym(e):

Acetylencarbamid, Acetylendiharnstoff, NSC 2765, Tetrahydroimidazo[4,5-d]imidazol-2,5-dion

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About This Item

Empirische Formel (Hill-System):
C4H6N4O2
CAS-Nummer:
Molekulargewicht:
142.12
Beilstein:
128826
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Qualitätsniveau

Assay

97%

mp (Schmelzpunkt)

>300 °C (lit.)

SMILES String

O=C1NC2NC(=O)NC2N1

InChI

1S/C4H6N4O2/c9-3-5-1-2(7-3)8-4(10)6-1/h1-2H,(H2,5,7,9)(H2,6,8,10)

InChIKey

VPVSTMAPERLKKM-UHFFFAOYSA-N

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Anwendung

Reactant involved in synthesis of:
  • Glycouril hexamers and monofunctionalized cucurbit[6]uril derivatives
  • N-chloro compounds from trichloroisocyanuric acid
  • Glycouril trimers

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Megha S Deshpande et al.
Bioconjugate chemistry, 20(3), 447-459 (2009-02-25)
Nine complexes of the type [Ru(N-N)(2)(BPG)]Cl(2) 1-4, [Ru(N-N)(BPG)(2)]Cl(2) 5-8, and [Ru(BPG)(3)]Cl(2) 9 where N-N is 2,2'-bipyridine (bpy), 1,10-phenanthroline (phen), dipyrido[3,2-d:2',3'-f]quinoxaline (dpq), dipyrido[3,2-a:2',3'-c]phenazine (dppz), which incorporates bipyridine-glycoluril (BPG-4b,5,7,7a-tetrahydro-4b,7a-epiminomethanoimino-6H-imidazo[4,5-f][1,10]phenanthroline-6,13-dione) as the ancillary ligand, have been synthesized and characterized. These complexes with the
Wolfgang-Andreas C Bauer et al.
Advanced materials (Deerfield Beach, Fla.), 23(45), 5404-5408 (2011-10-20)
Electron beam lithography is a powerful technique for the production of nanostructures but pattern quality depends on numerous interacting process variables. Orthogonal gradients of resist composition, baking temperatures, and development time as well as dose variations inside writing fields are
Dariush Ajami et al.
Journal of the American Chemical Society, 128(47), 15038-15039 (2006-11-23)
A cylindrical capsule containing a coiled alkane incorporates spacers. The alkane lengthens and gauche strain is relieved. The spacer can be removed to reset the system to the original state. The system represents a spring-loaded device that operates reversibly in
Derick Lucas et al.
Organic letters, 13(15), 4112-4115 (2011-07-12)
The fragmentation reaction of bis-nor-seco-CB[10] with 3,5-dimethylphenol (3) delivers methylene bridged glycoluril pentamer 5 in 81% yield. The host-guest recognition properties of the previously known tetramer 4 and those of pentamer 5 and hexamer 6 toward cationic guests in water
Arindam Chakraborty et al.
Journal of the American Chemical Society, 124(28), 8297-8306 (2002-07-11)
Cucurbit[6]uril (CB[6]) is a macrocyclic compound, prepared in one pot from glycoluril and formaldehyde, whose molecular recognition properties have made it the object of intense study. Studies of the mechanism of CB[n] formation, which might provide insights that allow the

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