454273
5-Ethyl-5-methylhydantoin
97%
Synonym(s):
5-Ethyl-5-methyl-2,4-imidazolidinedione, NSC 1020
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About This Item
Empirical Formula (Hill Notation):
C6H10N2O2
CAS Number:
Molecular Weight:
142.16
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
mp
144-150 °C (lit.)
SMILES string
CCC1(C)NC(=O)NC1=O
InChI
1S/C6H10N2O2/c1-3-6(2)4(9)7-5(10)8-6/h3H2,1-2H3,(H2,7,8,9,10)
InChI key
VSJRBQDMBFFHMC-UHFFFAOYSA-N
Application
Reactant for synthesis of nociceptin/orphanin FQ analogues
Certificates of Analysis (COA)
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Preferential crystallisation and comparative crystal growth study between pure enantiomer and racemic mixture of a chiral molecule: 5-ethyl-5-methylhydantoin.
Beilles S, et al.
Chemical Engineering Science, 56(7), 2281-2294 (2001)
Palash K Sarker et al.
International journal of molecular sciences, 13(1), 1006-1017 (2012-02-09)
Aqueous solutions of isovaline and its precursor molecule, 5-ethyl-5-methylhydantoin, were irradiated with ultraviolet and γ-ray photons, to evaluate their structural stability against space radiation. The degree of photolysis was measured and irradiation products were identified using chiral, reversed-phase and ion-exchange
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