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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
Management of the diffusion of 4-methylumbelliferone across phases in microdroplet-based systems for in vitro protein evolution.
2010-09
Comparison of current-use pesticide and other toxicant urinary metabolite levels among pregnant women in the CHAMACOS cohort and NHANES.
2010-06
High levels of miticides and agrochemicals in North American apiaries: implications for honey bee health.
2010-03-19
Evaluation of coumaphos exposure among tick eradication workers.
2010-02
Colony collapse disorder: a descriptive study.
2009-08-03
Biodegradation of coumaphos, chlorferon, and diethylthiophosphate using bacteria immobilized in Ca-alginate gel beads.
2009-02
Determination of diffusion coefficients and diffusion characteristics for chlorferon and diethylthiophosphate in Ca-alginate gel beads.
2008-07-01
Inhibitory potency against human acetylcholinesterase and enzymatic hydrolysis of fluorogenic nerve agent mimics by human paraoxonase 1 and squid diisopropyl fluorophosphatase.
2008-05-06
Dietary intake and its contribution to longitudinal organophosphorus pesticide exposure in urban/suburban children.
2008-04
Pesticide urinary metabolite levels of children in eastern North Carolina farmworker households.
2007-08
Organic diets significantly lower children's dietary exposure to organophosphorus pesticides.
2006-02
Analogues with fluorescent leaving groups for screening and selection of enzymes that efficiently hydrolyze organophosphorus nerve agents.
2006-01-12
Association of in utero organophosphate pesticide exposure and fetal growth and length of gestation in an agricultural population.
2004-07
Development of a simple and sensitive fluorimetric method for isolation of coumaphos-hydrolysing bacteria.
2002
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:24:03 GMT 2025
Edited
by admin
on Mon Mar 31 19:24:03 GMT 2025
Record UNII
EVI89HA9V3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-CHLORO-4-METHYL-7-HYDROXYCOUMARIN
Systematic Name English
NSC-24924
Preferred 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
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 Mon Mar 31 19:24:03 GMT 2025 , Edited by admin on Mon Mar 31 19:24:03 GMT 2025
PRIMARY
EPA CompTox
DTXSID8052724
Created by admin on Mon Mar 31 19:24:03 GMT 2025 , Edited by admin on Mon Mar 31 19:24:03 GMT 2025
PRIMARY
ECHA (EC/EINECS)
228-217-8
Created by admin on Mon Mar 31 19:24:03 GMT 2025 , Edited by admin on Mon Mar 31 19:24:03 GMT 2025
PRIMARY
NSC
24924
Created by admin on Mon Mar 31 19:24:03 GMT 2025 , Edited by admin on Mon Mar 31 19:24:03 GMT 2025
PRIMARY
MESH
C305311
Created by admin on Mon Mar 31 19:24:03 GMT 2025 , Edited by admin on Mon Mar 31 19:24:03 GMT 2025
PRIMARY
CAS
6174-86-3
Created by admin on Mon Mar 31 19:24:03 GMT 2025 , Edited by admin on Mon Mar 31 19:24:03 GMT 2025
PRIMARY
NSC
44204
Created by admin on Mon Mar 31 19:24:03 GMT 2025 , Edited by admin on Mon Mar 31 19:24:03 GMT 2025
PRIMARY
CHEBI
38620
Created by admin on Mon Mar 31 19:24:03 GMT 2025 , Edited by admin on Mon Mar 31 19:24:03 GMT 2025
PRIMARY
FDA UNII
EVI89HA9V3
Created by admin on Mon Mar 31 19:24:03 GMT 2025 , Edited by admin on Mon Mar 31 19:24:03 GMT 2025
PRIMARY
Related Record Type Details
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