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 |
|---|---|---|
| [PHARMACOLOGICAL ACTION OF TETRAHYDROFURFURYL 2-CARBAMOYLPHENOXYACETATE (PHENAMIDOFURYL)]. | 1963 Jan |
|
| [ON THE ANTIRHEUMATIC-ANTIARTHRITIC EFFECT OF PHENYLBUTAZONE AND PHENAMIDOFURYL IN PERCUTANEOUS ADMINISTRATION]. | 1964 Jan |
|
| [Spectrophotometric determination of single components of binary mixtures. I. Phenylbutazone and phenamidofuryl]. | 1965 Dec |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 17:50:35 UTC 2023
by
admin
on
Sat Dec 16 17:50:35 UTC 2023
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| Record UNII |
55408BLV3G
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
Download
| Name | Type | Language | ||
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Official Name | English | ||
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Systematic Name | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C241
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| Code System | Code | Type | Description | ||
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2075
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SUB07537MIG
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C65637
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735-64-8
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CHEMBL2104233
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55408BLV3G
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216212
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DTXSID70862394
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100000081261
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
