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Details

Stereochemistry ACHIRAL
Molecular Formula C9H11NO3
Molecular Weight 181.1885
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-METHOXYACETAMINOPHEN

SMILES

COC1=C(O)C=CC(NC(C)=O)=C1

InChI

InChIKey=KIZWIAQUWRXFNC-UHFFFAOYSA-N
InChI=1S/C9H11NO3/c1-6(11)10-7-3-4-8(12)9(5-7)13-2/h3-5,12H,1-2H3,(H,10,11)

HIDE SMILES / InChI

Molecular Formula C9H11NO3
Molecular Weight 181.1885
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
New analgesics synthetically derived from the paracetamol metabolite N-(4-hydroxyphenyl)-(5Z,8Z,11Z,14Z)-icosatetra-5,8,11,14-enamide.
2008-12-25
Dysmorphogenesis elicited by microinjected acetaminophen analogs and metabolites in rat embryos cultured in vitro.
1990-10
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:17:38 GMT 2025
Edited
by admin
on Mon Mar 31 19:17:38 GMT 2025
Record UNII
0GPW365VZ9
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-METHOXY-ACETAMINOPHEN
Preferred Name English
3-METHOXYACETAMINOPHEN
Common Name English
M-ACETANISIDIDE, 4'-HYDROXY-
Common Name English
4-ACETAMIDO-2-METHOXYPHENOL
Systematic Name English
ACETAMIDE, N-(4-HYDROXY-3-METHOXYPHENYL)-
Systematic Name English
3-METHOXYPARACETAMOL
Systematic Name English
Code System Code Type Description
MESH
C042796
Created by admin on Mon Mar 31 19:17:38 GMT 2025 , Edited by admin on Mon Mar 31 19:17:38 GMT 2025
PRIMARY
PUBCHEM
3080594
Created by admin on Mon Mar 31 19:17:38 GMT 2025 , Edited by admin on Mon Mar 31 19:17:38 GMT 2025
PRIMARY
EPA CompTox
DTXSID40186236
Created by admin on Mon Mar 31 19:17:38 GMT 2025 , Edited by admin on Mon Mar 31 19:17:38 GMT 2025
PRIMARY
CAS
3251-55-6
Created by admin on Mon Mar 31 19:17:38 GMT 2025 , Edited by admin on Mon Mar 31 19:17:38 GMT 2025
PRIMARY
FDA UNII
0GPW365VZ9
Created by admin on Mon Mar 31 19:17:38 GMT 2025 , Edited by admin on Mon Mar 31 19:17:38 GMT 2025
PRIMARY