G7305
Glycoluril
97%
Synonym(s):
Acetylene carbamide, Acetylenediurea, NSC 2765, Tetrahydroimidazo[4,5-d]imidazole-2,5-dione
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About This Item
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Quality Level
Assay
97%
mp
>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)
InChI key
VPVSTMAPERLKKM-UHFFFAOYSA-N
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Application
Reactant involved in synthesis of:
- Glycouril hexamers and monofunctionalized cucurbit[6]uril derivatives
- N-chloro compounds from trichloroisocyanuric acid
- Glycouril trimers
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Longer guests drive the reversible assembly of hyperextended capsules.
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A series of substituted glycoluril molecules exhibits a substantial twist of the fused five-membered rings and assembles exclusively chiral hydrogen-bonded ribbons in the solid-state.
Encapsulated carboxylic acid dimers with compressed hydrogen bonds.
Angewandte Chemie (International ed. in English), 50(2), 528-531 (2010-12-15)
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Synthetic receptors that surround their target molecules - self assembled capsules and deep cavitands - have emerged as the most realistic models of enzymes active sites. They were introduced to study the behaviour of molecules isolated in small spaces and
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