Home Other Building Blocks Ethyl iodoacetate

Ethyl iodoacetate

CAS No.:
623-48-3
Catalog Number:
AG00E9GG
Molecular Formula:
C4H7IO2
Molecular Weight:
214.0016
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Product Description
Catalog Number:
AG00E9GG
Chemical Name:
Ethyl iodoacetate
CAS Number:
623-48-3
Molecular Formula:
C4H7IO2
Molecular Weight:
214.0016
MDL Number:
MFCD00001081
IUPAC Name:
ethyl 2-iodoacetate
InChI:
InChI=1S/C4H7IO2/c1-2-7-4(6)3-5/h2-3H2,1H3
InChI Key:
MFFXVVHUKRKXCI-UHFFFAOYSA-N
SMILES:
CCOC(=O)CI
EC Number:
210-796-3
NSC Number:
58809
Properties
Complexity:
62.7  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
213.949g/mol
Formal Charge:
0
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
214.002g/mol
Monoisotopic Mass:
213.949g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
26.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.2  
Literature
Title Journal
Reactions of propargyl compounds containing a cyclobutyl group induced by a ruthenium complex. Chemistry, an Asian journal 20121101
Mixture toxicity of S(N)2-reactive soft electrophiles: 2-evaluation of mixtures containing ethyl α-halogenated acetates. Archives of environmental contamination and toxicology 20111101
Bisoxazolidine-catalyzed enantioselective Reformatsky reaction. The Journal of organic chemistry 20110805
Infrared spectroscopic studies of the conformation in ethyl alpha-haloacetates in the vapor, liquid and solid phases. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20100701
Catalytic enantioselective Reformatsky reaction with ortho-substituted diarylketones. Organic letters 20080918
Addition of electrophilic and heterocyclic carbon-centered radicals to glyoxylic oxime ethers. Organic letters 20040610
Properties