Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H6O2 |
| Molecular Weight | 86.0892 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C=CCOC=O
InChI
InChIKey=ZHHZHHSFKCANOC-UHFFFAOYSA-N
InChI=1S/C4H6O2/c1-2-3-6-4-5/h2,4H,1,3H2
| Molecular Formula | C4H6O2 |
| Molecular Weight | 86.0892 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Increased alpha1-fetoprotein production in rat liver injuries induced by various hepatotoxins. | 1976 Apr |
|
| Pro-oligonucleotide synthesis using allyl and allyloxycarbonyl protections: direct MALDI-TOF MS analysis on solid support. | 2001 Apr-Jul |
|
| An hypothesis for a mechanism underlying hepatotoxin-induced hypercreatinuria. | 2003 Apr |
|
| A stable bis-allyloxycarbonyl biotin aldehyde derivative for biotinylation via reductive alkylation: application to the synthesis of a biotinylated doxorubicin derivative. | 2003 Jan-Feb |
|
| Nucleobase protection with allyloxycarbonyl. | 2006 Jan |
|
| Synthesis of the 6-deoxytalose-containing tetrasaccharide of the glycopeptidolipid from Mycobacterium intracellare serotype 7. | 2008 Dec 8 |
|
| Synthesis of Macrocyclic Hexaoxazole (6OTD) Dimers, Containing Guanidine and Amine Functionalized Side Chains, and an Evaluation of Their Telomeric G4 Stabilizing Properties. | 2010 |
|
| Design, synthesis, and analysis of minor groove binder pyrrolepolyamide-2'-deoxyguanosine hybrids. | 2010 |
|
| Chiral-auxiliary-mediated 1,2-cis-glycosylations for the solid-supported synthesis of a biologically important branched alpha-glucan. | 2010 Jul |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:12:28 GMT 2023
by
admin
on
Fri Dec 15 19:12:28 GMT 2023
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| Record UNII |
A9WY6Q0U9C
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| Record Status |
Validated (UNII)
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| Record Version |
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