Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H9NO3 |
| Molecular Weight | 167.162 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)NC1=CC=C(O)C(O)=C1
InChI
InChIKey=IPFBMHOMTSBTSU-UHFFFAOYSA-N
InChI=1S/C8H9NO3/c1-5(10)9-6-2-3-7(11)8(12)4-6/h2-4,11-12H,1H3,(H,9,10)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Abnormal neurulation induced by 7-hydroxy-2-acetylaminofluorene and acetaminophen: evidence for catechol metabolites as proximate dysmorphogens. | 1989 Dec |
|
| Dysmorphogenesis elicited by microinjected acetaminophen analogs and metabolites in rat embryos cultured in vitro. | 1990 Oct |
|
| Advanced oxidation chemistry of paracetamol. UV/H(2)O(2)-induced hydroxylation/degradation pathways and (15)N-aided inventory of nitrogenous breakdown products. | 2002 Aug 23 |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
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Common Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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161950
Created by
admin on Fri Dec 15 17:52:04 GMT 2023 , Edited by admin on Fri Dec 15 17:52:04 GMT 2023
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PRIMARY | |||
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DTXSID50190960
Created by
admin on Fri Dec 15 17:52:04 GMT 2023 , Edited by admin on Fri Dec 15 17:52:04 GMT 2023
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IX22A3NJLN
Created by
admin on Fri Dec 15 17:52:04 GMT 2023 , Edited by admin on Fri Dec 15 17:52:04 GMT 2023
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37519-14-5
Created by
admin on Fri Dec 15 17:52:04 GMT 2023 , Edited by admin on Fri Dec 15 17:52:04 GMT 2023
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PRIMARY |
PARENT (METABOLITE)
SUBSTANCE RECORD
