Home Aldehydes 2-Oxiranecarboxaldehyde

2-Oxiranecarboxaldehyde

CAS No.:
765-34-4
Catalog Number:
AG005WZS
Molecular Formula:
C3H4O2
Molecular Weight:
72.0627
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Product Description
Catalog Number:
AG005WZS
Chemical Name:
2-Oxiranecarboxaldehyde
CAS Number:
765-34-4
Molecular Formula:
C3H4O2
Molecular Weight:
72.0627
MDL Number:
MFCD01724999
IUPAC Name:
oxirane-2-carbaldehyde
InChI:
InChI=1S/C3H4O2/c4-1-3-2-5-3/h1,3H,2H2
InChI Key:
IWYRWIUNAVNFPE-UHFFFAOYSA-N
SMILES:
C1OC1C=O
EC Number:
212-143-8
NSC Number:
521506
UN Number:
2622
Properties
Complexity:
50.9  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
72.021g/mol
Formal Charge:
0
Heavy Atom Count:
5  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
72.063g/mol
Monoisotopic Mass:
72.021g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
29.6A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.6  
Literature
Title Journal
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Formation and repair of tobacco carcinogen-derived bulky DNA adducts. Journal of nucleic acids 20100101
Substrate specificity of human thymine-DNA glycosylase on exocyclic cytosine adducts. Chemico-biological interactions 20070220
Treatment from birth of nonketotic hyperglycinemia due to a novel GLDC mutation. Annals of neurology 20060201
Alkylpurine-DNA-N-glycosylase excision of 7-(hydroxymethyl)-1,N6-ethenoadenine, a glycidaldehyde-derived DNA adduct. DNA repair 20060105
Effect of agmatine on heteromeric N-methyl-D-aspartate receptor channels. Neuroscience research 20050801
S-nitrosylation of N-ethylmaleimide sensitive factor mediates surface expression of AMPA receptors. Neuron 20050519
Effects of 1,3-butadiene, isoprene, and their photochemical degradation products on human lung cells. Environmental health perspectives 20041101
Structure of poly(propylene oxide) obtained with potassium glycidoxide in the presence of crown ether. Rapid communications in mass spectrometry : RCM 20040101
Novel activity of Escherichia coli mismatch uracil-DNA glycosylase (Mug) excising 8-(hydroxymethyl)-3,N4-ethenocytosine, a potential product resulting from glycidaldehyde reaction. Biochemistry 20020219
8-(Hydroxymethyl)-3,N(4)-etheno-C, a potential carcinogenic glycidaldehyde product, miscodes in vitro using mammalian DNA polymerases. Biochemistry 20020212
Properties