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Details

Stereochemistry ACHIRAL
Molecular Formula C10H7ClO3
Molecular Weight 210.614
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-CHLORO-4-METHYL-7-HYDROXYCOUMARIN

SMILES

CC1=C(Cl)C(=O)OC2=C1C=CC(O)=C2

InChI

InChIKey=ODZHLDRQCZXQFQ-UHFFFAOYSA-N
InChI=1S/C10H7ClO3/c1-5-7-3-2-6(12)4-8(7)14-10(13)9(5)11/h2-4,12H,1H3

HIDE SMILES / InChI

Molecular Formula C10H7ClO3
Molecular Weight 210.614
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Development of a simple and sensitive fluorimetric method for isolation of coumaphos-hydrolysing bacteria.
2002
Association of in utero organophosphate pesticide exposure and fetal growth and length of gestation in an agricultural population.
2004 Jul
Analogues with fluorescent leaving groups for screening and selection of enzymes that efficiently hydrolyze organophosphorus nerve agents.
2006 Jan 12
Inhibitory potency against human acetylcholinesterase and enzymatic hydrolysis of fluorogenic nerve agent mimics by human paraoxonase 1 and squid diisopropyl fluorophosphatase.
2008 May 6
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:52:57 GMT 2023
Edited
by admin
on Fri Dec 15 18:52:57 GMT 2023
Record UNII
EVI89HA9V3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-CHLORO-4-METHYL-7-HYDROXYCOUMARIN
Systematic Name English
CHLORFERRON
Common Name English
COUMARIN, 3-CHLORO-7-HYDROXY-4-METHYL-
Systematic Name English
NSC-44204
Code English
UMBELLIFERONE, 3-CHLORO-4-METHYL-
Common Name English
3-CHLORO-7-HYDROXY-4-METHYLCOUMARIN
Systematic Name English
3-CHLORO-7-HYDROXY-4-METHYL-2-BENZOPYRONE
Systematic Name English
7-HYDROXY-4-METHYL-3-CHLOROCOUMARIN
Systematic Name English
NSC-24924
Code English
2H-1-BENZOPYRAN-2-ONE, 3-CHLORO-7-HYDROXY-4-METHYL-
Systematic Name English
Code System Code Type Description
PUBCHEM
5355079
Created by admin on Fri Dec 15 18:52:57 GMT 2023 , Edited by admin on Fri Dec 15 18:52:57 GMT 2023
PRIMARY
EPA CompTox
DTXSID8052724
Created by admin on Fri Dec 15 18:52:57 GMT 2023 , Edited by admin on Fri Dec 15 18:52:57 GMT 2023
PRIMARY
ECHA (EC/EINECS)
228-217-8
Created by admin on Fri Dec 15 18:52:57 GMT 2023 , Edited by admin on Fri Dec 15 18:52:57 GMT 2023
PRIMARY
NSC
24924
Created by admin on Fri Dec 15 18:52:57 GMT 2023 , Edited by admin on Fri Dec 15 18:52:57 GMT 2023
PRIMARY
MESH
C305311
Created by admin on Fri Dec 15 18:52:57 GMT 2023 , Edited by admin on Fri Dec 15 18:52:57 GMT 2023
PRIMARY
CAS
6174-86-3
Created by admin on Fri Dec 15 18:52:57 GMT 2023 , Edited by admin on Fri Dec 15 18:52:57 GMT 2023
PRIMARY
NSC
44204
Created by admin on Fri Dec 15 18:52:57 GMT 2023 , Edited by admin on Fri Dec 15 18:52:57 GMT 2023
PRIMARY
CHEBI
38620
Created by admin on Fri Dec 15 18:52:57 GMT 2023 , Edited by admin on Fri Dec 15 18:52:57 GMT 2023
PRIMARY
FDA UNII
EVI89HA9V3
Created by admin on Fri Dec 15 18:52:57 GMT 2023 , Edited by admin on Fri Dec 15 18:52:57 GMT 2023
PRIMARY
Related Record Type Details
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