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Details

Stereochemistry ACHIRAL
Molecular Formula C8H8O4
Molecular Weight 168.1467
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-HYDROXY-3-METHOXYBENZOIC ACID

SMILES

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

InChI

InChIKey=AUZQQIPZESHNMG-UHFFFAOYSA-N
InChI=1S/C8H8O4/c1-12-6-4-2-3-5(7(6)9)8(10)11/h2-4,9H,1H3,(H,10,11)

HIDE SMILES / InChI

Molecular Formula C8H8O4
Molecular Weight 168.1467
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
2-Hydr-oxy-3-methoxy-benzoic acid monohydrate.
2008-03-12
Doxorubicin inhibits oxidation of 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonate) (ABTS) by a lactoperoxidase/H(2)O(2) system by reacting with ABTS-derived radical.
2007-10-15
Inactivation of anthracyclines by serum heme proteins.
2007-06
Inactivation of anthracyclines by cellular peroxidase.
2005-07-15
The enhancement of riboflavin-mediated photo-oxidation of doxorubicin by histidine and urocanic acid.
2001-04
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 20:39:38 GMT 2025
Edited
by admin
on Mon Mar 31 20:39:38 GMT 2025
Record UNII
3J31Y0E2IM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-134533
Preferred Name English
2-HYDROXY-3-METHOXYBENZOIC ACID
Systematic Name English
O-VANILLIC ACID
Common Name English
NSC-408167
Code English
BENZOIC ACID, 2-HYDROXY-3-METHOXY-
Common Name English
3-METHOXYSALICYLIC ACID
Systematic Name English
SALICYLIC ACID, 3-METHOXY-
Common Name English
3-METHOXY-2-HYDROXYBENZOIC ACID
Systematic Name English
M-ANISIC ACID, 2-HYDROXY-
Common Name English
Code System Code Type Description
PUBCHEM
70140
Created by admin on Mon Mar 31 20:39:38 GMT 2025 , Edited by admin on Mon Mar 31 20:39:38 GMT 2025
PRIMARY
ECHA (EC/EINECS)
212-888-9
Created by admin on Mon Mar 31 20:39:38 GMT 2025 , Edited by admin on Mon Mar 31 20:39:38 GMT 2025
PRIMARY
CHEBI
68496
Created by admin on Mon Mar 31 20:39:38 GMT 2025 , Edited by admin on Mon Mar 31 20:39:38 GMT 2025
PRIMARY
FDA UNII
3J31Y0E2IM
Created by admin on Mon Mar 31 20:39:38 GMT 2025 , Edited by admin on Mon Mar 31 20:39:38 GMT 2025
PRIMARY
EPA CompTox
DTXSID20236566
Created by admin on Mon Mar 31 20:39:38 GMT 2025 , Edited by admin on Mon Mar 31 20:39:38 GMT 2025
PRIMARY
NSC
134533
Created by admin on Mon Mar 31 20:39:38 GMT 2025 , Edited by admin on Mon Mar 31 20:39:38 GMT 2025
PRIMARY
NSC
408167
Created by admin on Mon Mar 31 20:39:38 GMT 2025 , Edited by admin on Mon Mar 31 20:39:38 GMT 2025
PRIMARY
CAS
877-22-5
Created by admin on Mon Mar 31 20:39:38 GMT 2025 , Edited by admin on Mon Mar 31 20:39:38 GMT 2025
PRIMARY