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About This Item
Empirical Formula (Hill Notation):
C5H8N2O2
CAS Number:
Molecular Weight:
128.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-051-3
Beilstein/REAXYS Number:
2827
MDL number:
Assay:
97%
Form:
crystals
Product Name
5,5-Dimethylhydantoin, 97%
InChI key
YIROYDNZEPTFOL-UHFFFAOYSA-N
InChI
1S/C5H8N2O2/c1-5(2)3(8)6-4(9)7-5/h1-2H3,(H2,6,7,8,9)
SMILES string
CC1(C)NC(=O)NC1=O
assay
97%
form
crystals
mp
174-177 °C (lit.)
Quality Level
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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
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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During long-term lung infection in cystic fibrosis (CF) patients, Burkholderia cenocepacia faces multiple selective pressures in this highly stressful and fluctuating environment. As a consequence, the initial infecting strain undergoes genetic changes that result in the diversification of genotypes and
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CBT is considered the first-line treatment for anxiety disorders, particularly when it involves gradual confrontation with feared stimuli (i.e., exposure); however, delivery of CBT for anxiety disorders in real-world community clinics is lacking. This study utilized surveys we developed with
Joseph Jacob et al.
BMC medicine, 14(1), 190-190 (2016-11-24)
To evaluate computer-based computer tomography (CT) analysis (CALIPER) against visual CT scoring and pulmonary function tests (PFTs) when predicting mortality in patients with connective tissue disease-related interstitial lung disease (CTD-ILD). To identify outcome differences between distinct CTD-ILD groups derived following
Umit Makal et al.
Biomaterials, 27(8), 1316-1326 (2005-09-27)
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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