524832
2-Oxo-1-imidazolidinecarbonyl chloride
96%
Synonym(s):
Ethyleneallophanoyl chloride
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C4H5ClN2O2
CAS Number:
Molecular Weight:
148.55
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
236-185-1
MDL number:
Assay:
96%
InChI key
NXJZQSRAFBHNLI-UHFFFAOYSA-N
InChI
1S/C4H5ClN2O2/c5-3(8)7-2-1-6-4(7)9/h1-2H2,(H,6,9)
SMILES string
ClC(=O)N1CCNC1=O
assay
96%
mp
147-151 °C (lit.)
functional group
chloro
Quality Level
General description
2-Oxo-1-imidazolidinecarbonyl chloride (Ethyleneallophanoyl chloride) is an imidazoline derivative. It is a straight-chain allophanoyl chloride.
Application
Reactant for ytterbium metal promoted reactions
Reactant for synthesis of selenoesters by samarium diiodide induced reductive cleavage of Se-Se bonds
Reactant for synthesis of selenoesters by samarium diiodide induced reductive cleavage of Se-Se bonds
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
The Dehydrochlorination of Allophanoyl Chlorides. A New Synthesis of Isocyanates.
Sayigh AAR, et al.
The Journal of Organic Chemistry, 29(11), 3344- 3347 (1964)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service