I601
2-Imidazolidone
96%
Synonym(s):
2-Oxoimidazolidine, N,N′-Ethyleneurea
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About This Item
Empirical Formula (Hill Notation):
C3H6N2O
CAS Number:
Molecular Weight:
86.09
Beilstein:
106252
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
96%
mp
129-132 °C (lit.)
SMILES string
O=C1NCCN1
InChI
1S/C3H6N2O/c6-3-4-1-2-5-3/h1-2H2,(H2,4,5,6)
InChI key
YAMHXTCMCPHKLN-UHFFFAOYSA-N
Gene Information
human ... EPHX2(2053)
mouse ... Ephx2(13850)
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Application
Reactant for synthesis of:
Reactant for:
- Chiral microporous materials from achiral precursors
- Aryl and heteroaryl N-acylureas via microwave-assisted palladium-catalyzed carbonylation
- A highly water-soluble peptide based human neutrophil elastase inhibitor
- Heterocycles by cyanoacetylation for antimicrobial use
Reactant for:
- Pd-catalyzed C-N bond formation with heteroaromatic tosylates
- Oxidative amidation of activated alkenes
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - STOT RE 2
Target Organs
Thyroid
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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A series of peptide-based transition-state human neutrophil elastase (HNE) inhibitors with N-terminal acidic moieties were synthesized and their inhibitory activity against HNE was evaluated both in vitro and in vivo. Our results show that compounds containing cyclic amide bridged acidic
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Mette L H Mantel et al.
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A protocol for the palladium(0)-catalyzed amidation of heteroaromatic tosylates was successfully developed. The methodology proved to be effective for a variety of heteroaryl tosylates including the pyridine, pyrimidine, quinoline and quinoxaline ring systems. Successful carbon-nitrogen bond formation with these heteroaryl
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