Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H14O2 |
| Molecular Weight | 130.1849 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOC(OCC)C=C
InChI
InChIKey=MCIPQLOKVXSHTD-UHFFFAOYSA-N
InChI=1S/C7H14O2/c1-4-7(8-5-2)9-6-3/h4,7H,1,5-6H2,2-3H3
| Molecular Formula | C7H14O2 |
| Molecular Weight | 130.1849 |
| 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 |
|---|---|---|
| Opening of thiiranes: preparation of orthogonal protected 2-thioglyceraldehyde. | 2001 Feb 9 |
|
| An efficient palladium-catalyzed synthesis of cinnamaldehydes from acrolein diethyl acetal and aryl iodides and bromides. | 2003 Mar 6 |
|
| Nickel-catalyzed arylation of acrolein diethyl acetal: a substitute to the 1,4-addition of arylhalides to acrolein. | 2003 Nov 27 |
|
| Part 3. Triethylborane-air: a suitable initiator for intermolecular radical additions of S-2-oxoalkyl-thionocarbonates (S-xanthates) to olefins. | 2007 Dec 13 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:34:08 GMT 2023
by
admin
on
Fri Dec 15 17:34:08 GMT 2023
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| Record UNII |
33XN703369
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| Record Status |
Validated (UNII)
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| Record Version |
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3054-95-3
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33XN703369
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62477
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221-276-0
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DTXSID0020024
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C054119
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60135
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