19940
N-Butylurea
purum, ≥99.0% (N)
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About This Item
Linear Formula:
CH3(CH2)3NHCONH2
CAS Number:
Molecular Weight:
116.16
EC Number:
209-748-4
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1744775
MDL number:
grade
purum
assay
≥99.0% (N)
mp
95-98 °C
SMILES string
CCCCNC(N)=O
InChI
1S/C5H12N2O/c1-2-3-4-7-5(6)8/h2-4H2,1H3,(H3,6,7,8)
InChI key
CNWSQCLBDWYLAN-UHFFFAOYSA-N
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Peter L Larsen et al.
Journal of the American Chemical Society, 126(21), 6522-6523 (2004-05-27)
Metal complexes with terminal chalcogenido ligands are known for the early transition-metal complexes, yet for the heavier congeners (e.g., sulfido and selenido), there are no analogous examples for the late 3d metal ions. Reported herein is the isolation and characterization
Kevin X Chen et al.
Bioorganic & medicinal chemistry, 16(4), 1874-1883 (2007-11-23)
Starting from a pentapeptide Hepatitis C virus NS3 protease inhibitor, a number of alpha-ketoamide inhibitors based on novel dichlorocyclopropylproline P2 core were synthesized and investigated for their HCV NS3 serine protease activity. The key intermediate 3,4-dichlorocyclopropylproline was obtained through a
Thermodynamics of anti-sickling agents with hemoglobin S.
R C Benedict et al.
Journal of molecular biology, 150(3), 423-434 (1981-08-15)
Taiho Park et al.
Journal of the American Chemical Society, 127(51), 18133-18142 (2005-12-22)
An exceptionally strong quadruply hydrogen-bonded complex is formed between 2,7-diamido-1,8-naphthyridine 3 (DAN) and the butylurea of guanosine 6 (UG) in chloroform. The UG unit can be prepared in four steps from guanosine on a 10 g scale in excellent yields
Ai Ito et al.
Chemical & pharmaceutical bulletin, 58(1), 82-86 (2010-01-05)
Otherwise inaccessible tropolonylureas were prepared by reaction of t-butylurea with appropriate amines, with elimination of t-butylamine. This method is also generally applicable for urea synthesis.
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