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About This Item
Empirical Formula (Hill Notation):
C5H6N2O4
CAS Number:
Molecular Weight:
158.11
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
226-574-4
MDL number:
Assay:
98%
Form:
powder
InChI key
DQQLZADYSWBCOX-UHFFFAOYSA-N
InChI
1S/C5H6N2O4/c8-3(9)1-2-4(10)7-5(11)6-2/h2H,1H2,(H,8,9)(H2,6,7,10,11)
SMILES string
OC(=O)CC1NC(=O)NC1=O
assay
98%
form
powder
mp
214-215 °C (dec.) (lit.)
functional group
carboxylic acid
Application
Reactant for synthesis of:
- Nonfolate compounds as antiparasitic agents inhibiting pteridine reductase
- 2,4-Azolidinedione-acetic acid derivatives as anticancer agents
- Anti-inflammatory and analgesic drugs
- Amides via polystyrene-supported N-hydroxybenxotriazole resin
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Marta Chylińska et al.
Molecules (Basel, Switzerland), 25(16) (2020-08-23)
Current demand for new protective materials ensuring sterility is systematically growing. The purpose of this work was the synthesis of the biocidal N-halamine hydantoin-containing chitosan (CS-CMH-Cl) and characterization of its properties. The functionalization of the chitosan by 5-hydantoinacetic acid substitution
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