Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H10O3 |
| Molecular Weight | 166.1739 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)COC1=CC=CC=C1
InChI
InChIKey=BZCKRPHEZOHHBK-UHFFFAOYSA-N
InChI=1S/C9H10O3/c1-11-9(10)7-12-8-5-3-2-4-6-8/h2-6H,7H2,1H3
| Molecular Formula | C9H10O3 |
| Molecular Weight | 166.1739 |
| 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 |
|---|---|---|
| Dicarboxylic degradation products of nonylphenol polyethoxylates: synthesis and identification by gas chromatography-mass spectrometry using electron and chemical ionization modes. | 2004-12-17 |
|
| Combinatorial formulation of biocatalyst preparations for increased activity in organic solvents: salt activation of penicillin amidase. | 2004-03-05 |
|
| Synthesis of functionalized porphyrins as oxygen ligand receptors. | 2003-06-27 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:09:44 GMT 2025
by
admin
on
Mon Mar 31 22:09:44 GMT 2025
|
| Record UNII |
JD9OF3328O
|
| Record Status |
Validated (UNII)
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| Record Version |
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16365
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JD9OF3328O
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2065-23-8
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DTXSID2062161
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32414
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218-176-4
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