Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C14H17NO5 |
| Molecular Weight | 279.2885 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=O)C1=CC=CC=C1OCC(=O)OCC2CCCO2
InChI
InChIKey=CNANHKGYHBTGAQ-UHFFFAOYSA-N
InChI=1S/C14H17NO5/c15-14(17)11-5-1-2-6-12(11)19-9-13(16)20-8-10-4-3-7-18-10/h1-2,5-6,10H,3-4,7-9H2,(H2,15,17)
| Molecular Formula | C14H17NO5 |
| Molecular Weight | 279.2885 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
PubMed
| Title | Date | PubMed |
|---|---|---|
| [Spectrophotometric determination of single components of binary mixtures. I. Phenylbutazone and phenamidofuryl]. | 1965-12 |
|
| [ON THE ANTIRHEUMATIC-ANTIARTHRITIC EFFECT OF PHENYLBUTAZONE AND PHENAMIDOFURYL IN PERCUTANEOUS ADMINISTRATION]. | 1964-01 |
|
| [PHARMACOLOGICAL ACTION OF TETRAHYDROFURFURYL 2-CARBAMOYLPHENOXYACETATE (PHENAMIDOFURYL)]. | 1963-01 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 09:39:50 GMT 2025
by
admin
on
Wed Apr 02 09:39:50 GMT 2025
|
| Record UNII |
55408BLV3G
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Official Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C241
Created by
admin on Wed Apr 02 09:39:50 GMT 2025 , Edited by admin on Wed Apr 02 09:39:50 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
2075
Created by
admin on Wed Apr 02 09:39:50 GMT 2025 , Edited by admin on Wed Apr 02 09:39:50 GMT 2025
|
PRIMARY | |||
|
SUB07537MIG
Created by
admin on Wed Apr 02 09:39:50 GMT 2025 , Edited by admin on Wed Apr 02 09:39:50 GMT 2025
|
PRIMARY | |||
|
C65637
Created by
admin on Wed Apr 02 09:39:50 GMT 2025 , Edited by admin on Wed Apr 02 09:39:50 GMT 2025
|
PRIMARY | |||
|
735-64-8
Created by
admin on Wed Apr 02 09:39:50 GMT 2025 , Edited by admin on Wed Apr 02 09:39:50 GMT 2025
|
PRIMARY | |||
|
CHEMBL2104233
Created by
admin on Wed Apr 02 09:39:50 GMT 2025 , Edited by admin on Wed Apr 02 09:39:50 GMT 2025
|
PRIMARY | |||
|
55408BLV3G
Created by
admin on Wed Apr 02 09:39:50 GMT 2025 , Edited by admin on Wed Apr 02 09:39:50 GMT 2025
|
PRIMARY | |||
|
216212
Created by
admin on Wed Apr 02 09:39:50 GMT 2025 , Edited by admin on Wed Apr 02 09:39:50 GMT 2025
|
PRIMARY | |||
|
DTXSID70862394
Created by
admin on Wed Apr 02 09:39:50 GMT 2025 , Edited by admin on Wed Apr 02 09:39:50 GMT 2025
|
PRIMARY | |||
|
100000081261
Created by
admin on Wed Apr 02 09:39:50 GMT 2025 , Edited by admin on Wed Apr 02 09:39:50 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ENANTIOMER -> RACEMATE | |||
|
|
ENANTIOMER -> RACEMATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |