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
Beilstein:
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 Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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The inherent antimicrobial properties and biodegradability of chitosan make it an ideal candidate for antimicrobial materials. In this study, N-halamine precursor 3-glycidyl-5,5-dimethylhydantoin (GH) was synthesized and bonded onto chitosan by a ring opening reaction between chitosan and GH. The chitosan
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Endosulfan (ENDO) is a widely used organochlorine (OC) pesticide and persistent organo-pollutant. Epidemiological studies have shown that high levels of OC exposure were related to colorectal cancer (CRC) incidence. The objectives of the present study were to evaluate histological changes
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