D161403
5,5-Dimethylhydantoin
97%
Synonym(s):
Fennosurf 300, 4,4-Dimethyl-2,5-dioxoimidazolidine, DMH
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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
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
Quality Level
Related Categories
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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