524832
2-Oxo-1-imidazolidinecarbonyl chloride
96%
Synonym(s):
Ethyleneallophanoyl chloride
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C4H5ClN2O2
CAS Number:
Molecular Weight:
148.55
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
96%
mp
147-151 °C (lit.)
SMILES string
ClC(=O)N1CCNC1=O
InChI
1S/C4H5ClN2O2/c5-3(8)7-2-1-6-4(7)9/h1-2H2,(H,6,9)
InChI key
NXJZQSRAFBHNLI-UHFFFAOYSA-N
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
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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