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About This Item
Empirical Formula (Hill Notation):
C5H6N2O2
CAS Number:
Molecular Weight:
126.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-949-4
Beilstein/REAXYS Number:
115647
MDL number:
Assay:
97%
Form:
powder
Quality Level
assay
97%
form
powder
mp
318 °C (dec.) (lit.)
SMILES string
CC1=CC(=O)NC(=O)N1
InChI
1S/C5H6N2O2/c1-3-2-4(8)7-5(9)6-3/h2H,1H3,(H2,6,7,8,9)
InChI key
SHVCSCWHWMSGTE-UHFFFAOYSA-N
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Fabio C Tucci et al.
Bioorganic & medicinal chemistry letters, 13(19), 3317-3322 (2003-09-03)
A new class of small molecule GnRH antagonists, the 1-arylmethyl-3-(1-methyl-2-amino)ethyl-5-aryl-6-methyluracils, was designed and a novel stereoselective synthesis for these compounds was developed. The stereochemical integrities of key intermediates (S)-6 and (R)-6 were confirmed by a combination of X-ray crystallography and
Adrian Häberli et al.
Nucleosides, nucleotides & nucleic acids, 22(5-8), 1187-1189 (2003-10-21)
We synthesized pyrrolidino-C-nucleosides, incorporated them into oligodeoxynucleotides and investigated their pairing properties. The thermal duplex and triplex stabilities were measured. While triplex formation is destabilized in the case of pyrrolidino-pseudo-U and -T, pyrrolidino-pseudo-iso-C leads to an increase of the Tm
Effect of tetraalkylammonium derivatives of 6-methyluracil on the endplate potentials of muscles of different functional types.
I V Kovyazina et al.
Doklady biological sciences : proceedings of the Academy of Sciences of the USSR, Biological sciences sections, 399, 458-460 (2005-02-19)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| D115207-100G | 04061832917443 |
