Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C11H12O3 |
| Molecular Weight | 192.2112 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)\C=C\C1=CC=C(OC)C=C1
InChI
InChIKey=VEZIKIAGFYZTCI-VMPITWQZSA-N
InChI=1S/C11H12O3/c1-13-10-6-3-9(4-7-10)5-8-11(12)14-2/h3-8H,1-2H3/b8-5+
| Molecular Formula | C11H12O3 |
| Molecular Weight | 192.2112 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| The anise-like odor of Clitocybe odora, Lentinellus cochleatus and Agaricus essettei. | 2010-12-16 |
|
| [Antifungal sctivities and stability of extracts from culture liquid of Hypoxylon perforatum to Sphaeropsis sapinea]. | 2009-07 |
|
| The genome-wide expression profile of Scrophularia ningpoensis-treated thapsigargin-stimulated U-87MG cells. | 2009-05 |
|
| VCD configuration of enantiopure/-enriched tetrasubstituted alpha-fluoro cyclohexanones and their use for epoxidation of trans-olefins. | 2004-08 |
|
| A catalytic asymmetric synthesis of chiral glycidic acid derivatives through chiral dioxirane-mediated catalytic asymmetric epoxidation of cinnamic acid derivatives. | 2004-06-11 |
|
| New anthraquinones from Gladiolus gandavensis. | 2003-12 |
|
| A practical procedure for the large-scale preparation of methyl (2R,3S)-3-(4-methoxyphenyl)glycidate, a key intermediate for diltiazem. | 2002-06-28 |
|
| Methyl 3-(4-methoxyphenyl)prop-2-enoate. | 2002-02 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:55:25 GMT 2025
by
admin
on
Mon Mar 31 18:55:25 GMT 2025
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| Record UNII |
1F58T0S3Q7
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| Record Status |
Validated (UNII)
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| Record Version |
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223-455-9
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832-01-9
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1F58T0S3Q7
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26461
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3901-07-3
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DTXSID401312296
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641297
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212-614-8
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ALTERNATIVE |