Details
| Stereochemistry | UNKNOWN |
| Molecular Formula | C12H14O3 |
| Molecular Weight | 206.2378 |
| Optical Activity | ( - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC1CC2=C(O1)C=CC(CC(O)=O)=C2
InChI
InChIKey=MYQXHLQMZLTSDB-UHFFFAOYSA-N
InChI=1S/C12H14O3/c1-2-10-7-9-5-8(6-12(13)14)3-4-11(9)15-10/h3-5,10H,2,6-7H2,1H3,(H,13,14)
| Molecular Formula | C12H14O3 |
| Molecular Weight | 206.2378 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Metabolites and analogs of 2-ethyl-2,3-dihydro-5-benzofuranacetic acid (furofenac): chemical and pharmacological properties. | 1980 Feb |
|
| Mass spectrometry of the metabolites of 2-ethyl-2,3-dihydro-5-benzofuranylacetic acid. | 1980 Jun |
|
| Effect of SAS 650 (Furofenac) on malondialydehyde production by platelets. | 1984 Jun |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 06:51:53 UTC 2023
by
admin
on
Sat Dec 16 06:51:53 UTC 2023
|
| Record UNII |
9EP849A4GR
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| Record Status |
Validated (UNII)
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| Record Version |
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-
Download
| Name | Type | Language | ||
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Common Name | English |
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200959-06-4
Created by
admin on Sat Dec 16 06:51:53 UTC 2023 , Edited by admin on Sat Dec 16 06:51:53 UTC 2023
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PRIMARY | |||
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9EP849A4GR
Created by
admin on Sat Dec 16 06:51:53 UTC 2023 , Edited by admin on Sat Dec 16 06:51:53 UTC 2023
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ENANTIOMER -> ENANTIOMER |
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RACEMATE -> ENANTIOMER |
