Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H8O3 |
| Molecular Weight | 152.1473 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC(C(O)=O)=C(O)C=C1
InChI
InChIKey=DLGBEGBHXSAQOC-UHFFFAOYSA-N
InChI=1S/C8H8O3/c1-5-2-3-7(9)6(4-5)8(10)11/h2-4,9H,1H3,(H,10,11)
| Molecular Formula | C8H8O3 |
| Molecular Weight | 152.1473 |
| 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 |
|---|---|---|
| Biochemical and molecular characterization of a ring fission dioxygenase with the ability to oxidize (substituted) salicylate(s) from Pseudaminobacter salicylatoxidans. | 2004 Sep 3 |
|
| Catabolic role of a three-component salicylate oxygenase from Sphingomonas yanoikuyae B1 in polycyclic aromatic hydrocarbon degradation. | 2005 Feb 18 |
|
| Self-assembly of surfactant vesicles that transform into viscoelastic wormlike micelles upon heating. | 2006 May 24 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 02:08:37 GMT 2023
by
admin
on
Sat Dec 16 02:08:37 GMT 2023
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| Record UNII |
6GAI2MTV5V
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| Record Status |
Validated (UNII)
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| Record Version |
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89-56-5
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m3841
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admin on Sat Dec 16 02:08:37 GMT 2023 , Edited by admin on Sat Dec 16 02:08:37 GMT 2023
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38518
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6GAI2MTV5V
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DTXSID20237472
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6973
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201-918-6
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5-Methoxysalicylic acid
Created by
admin on Sat Dec 16 02:08:37 GMT 2023 , Edited by admin on Sat Dec 16 02:08:37 GMT 2023
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