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Details

Stereochemistry RACEMIC
Molecular Formula C14H13HgO5.HO
Molecular Weight 478.85
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MERCUMALLYLIC ACID

SMILES

[OH-].COC(C[Hg+])CC1=CC=CC2=C1OC(=O)C(=C2)C(O)=O

InChI

InChIKey=VMNRZYKMPOZISX-UHFFFAOYSA-M
InChI=1S/C14H13O5.Hg.H2O/c1-8(18-2)6-9-4-3-5-10-7-11(13(15)16)14(17)19-12(9)10;;/h3-5,7-8H,1,6H2,2H3,(H,15,16);;1H2/q;+1;/p-1

HIDE SMILES / InChI

Approval Year

Unknown
149124
Name Type Language
(3-(3-(HYDROXYMERCURI)-2-METHOXYPROPYL)SALICYLIDENE)MALONIC ACID .DELTA.-LACTONE
Preferred Name English
MERCUMALLYLIC ACID
MI  
Common Name English
8-(3-(HYDROXYMERCURI)-2-METHOXYPROPYL)-2-OXO-2H-1-BENZOPYRAN-3-CARBOXYLIC ACID
Common Name English
8-(3-(HYDROXYMERCURI)-2-METHOXYPROPYL)-3-CARBOXYCOUMARIN
Common Name English
MERCUMALLIC ACID
Common Name English
8-(2-METHOXY-3-HYDROXYMERCURIPROPYL)COUMARIN-3-CARBOXYLIC ACID
Common Name English
(3-(3-CARBOXY-2-OXO-2H-1-BENZOPYRAN-8-YL)-2-METHOXYPROPYL)HYDROXYMERCURATE(1-) HYDROGEN (1:1)
Common Name English
8-(3-(HYDROXYMERCURI)-2-METHOXYPROPYL)COUMARIN-3-CARBOXYLIC ACID
Common Name English
MERCURATE(1-), (3-(3-CARBOXYLATO-2-OXO-2H-1-BENZOPYRAN-8-YL)-2-METHOXYPROPYL)HYDROXY-, HYDROGEN (1:1)
Common Name English
MERCUMALLYLIC ACID [MI]
Common Name English
Code System Code Type Description
FDA UNII
2247QE21F1
Created by admin on Mon Mar 31 17:45:06 GMT 2025 , Edited by admin on Mon Mar 31 17:45:06 GMT 2025
PRIMARY
PUBCHEM
101603130
Created by admin on Mon Mar 31 17:45:06 GMT 2025 , Edited by admin on Mon Mar 31 17:45:06 GMT 2025
PRIMARY
EPA CompTox
DTXSID601018981
Created by admin on Mon Mar 31 17:45:06 GMT 2025 , Edited by admin on Mon Mar 31 17:45:06 GMT 2025
PRIMARY
CAS
86-36-2
Created by admin on Mon Mar 31 17:45:06 GMT 2025 , Edited by admin on Mon Mar 31 17:45:06 GMT 2025
PRIMARY
MERCK INDEX
m7209
Created by admin on Mon Mar 31 17:45:06 GMT 2025 , Edited by admin on Mon Mar 31 17:45:06 GMT 2025
PRIMARY Merck Index
SUBSTANCE RECORD
Structure of MERCUMALLYLIC ACID
NIH
NCATS
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