D161403
5,5-Dimethylhydantoin
97%
Sinónimos:
Fennosurf 300, 4,4-Dimethyl-2,5-dioxoimidazolidine, DMH
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About This Item
Fórmula empírica (notación de Hill):
C5H8N2O2
Número de CAS:
Peso molecular:
128.13
Beilstein/REAXYS Number:
2827
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
97%
form
crystals
mp
174-177 °C (lit.)
SMILES string
CC1(C)NC(=O)NC1=O
InChI
1S/C5H8N2O2/c1-5(2)3(8)6-4(9)7-5/h1-2H3,(H2,6,7,8,9)
InChI key
YIROYDNZEPTFOL-UHFFFAOYSA-N
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Application
Reactant for synthesis of:
Reactant for asymmetric chlorolactonization reactions
- N-chloroheterocyclic antimicrobials
- β-Amino alcohols as inhibitors of antitubercular target N-acetyltransferase
- Second-generation selective inhibitors of hepatitis C virus NS3 serine protease
- Rechargeable biocidal cellulose
- N-chlorohydantoins
Reactant for asymmetric chlorolactonization reactions
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Polyurethanes (PUs) with soft blocks containing semifluorinated (-CH2OCH2CF3) and 5,5-dimethylhydantoin pendant groups were prepared and employed (2 wt%) as biocidal polymeric surface modifiers (PSMs) for a conventional PU coating comprised of an isophorone diisocyanate/1,4-butanediol-derived hard block (50%) and poly(tetramethylene oxide)
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