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Details

Stereochemistry ACHIRAL
Molecular Formula C8H8O3
Molecular Weight 152.1473
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of P-CRESOTIC ACID

SMILES

CC1=CC(C(O)=O)=C(O)C=C1

InChI

InChIKey=DLGBEGBHXSAQOC-UHFFFAOYSA-N
InChI=1S/C8H8O3/c1-5-2-3-7(9)6(4-5)8(10)11/h2-4,9H,1H3,(H,10,11)

HIDE SMILES / InChI

Molecular Formula C8H8O3
Molecular Weight 152.1473
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Biochemical and molecular characterization of a ring fission dioxygenase with the ability to oxidize (substituted) salicylate(s) from Pseudaminobacter salicylatoxidans.
2004 Sep 3
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 02:08:37 GMT 2023
Edited
by admin
on Sat Dec 16 02:08:37 GMT 2023
Record UNII
6GAI2MTV5V
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
P-CRESOTIC ACID
MI  
Common Name English
6-HYDROXY-M-TOLUIC ACID
Systematic Name English
P-CRESOTIC ACID [MI]
Common Name English
P-CRESOTINIC ACID
Common Name English
6-HYDROXY-3-METHYLBENZOIC ACID
Systematic Name English
2,5-CRESOTIC ACID
Common Name English
NSC-38518
Code English
.ALPHA.-CRESOTINIC ACID
Common Name English
5-METHYLSALICYLIC ACID
Systematic Name English
5-METHYL-2-HYDROXYBENZOIC ACID
Systematic Name English
P-HOMOSALICYLIC ACID
Common Name English
2-HYDROXY-5-METHYLBENZOIC ACID
Systematic Name English
Code System Code Type Description
CAS
89-56-5
Created by admin on Sat Dec 16 02:08:37 GMT 2023 , Edited by admin on Sat Dec 16 02:08:37 GMT 2023
PRIMARY
MERCK INDEX
m3841
Created by admin on Sat Dec 16 02:08:37 GMT 2023 , Edited by admin on Sat Dec 16 02:08:37 GMT 2023
PRIMARY Merck Index
NSC
38518
Created by admin on Sat Dec 16 02:08:37 GMT 2023 , Edited by admin on Sat Dec 16 02:08:37 GMT 2023
PRIMARY
FDA UNII
6GAI2MTV5V
Created by admin on Sat Dec 16 02:08:37 GMT 2023 , Edited by admin on Sat Dec 16 02:08:37 GMT 2023
PRIMARY
EPA CompTox
DTXSID20237472
Created by admin on Sat Dec 16 02:08:37 GMT 2023 , Edited by admin on Sat Dec 16 02:08:37 GMT 2023
PRIMARY
PUBCHEM
6973
Created by admin on Sat Dec 16 02:08:37 GMT 2023 , Edited by admin on Sat Dec 16 02:08:37 GMT 2023
PRIMARY
ECHA (EC/EINECS)
201-918-6
Created by admin on Sat Dec 16 02:08:37 GMT 2023 , Edited by admin on Sat Dec 16 02:08:37 GMT 2023
PRIMARY
WIKIPEDIA
5-Methoxysalicylic acid
Created by admin on Sat Dec 16 02:08:37 GMT 2023 , Edited by admin on Sat Dec 16 02:08:37 GMT 2023
PRIMARY