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Details

Stereochemistry RACEMIC
Molecular Formula C12H15NO4
Molecular Weight 237.2518
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-HYDROXYCARBOFURAN

SMILES

CNC(=O)OC1=CC=CC2=C1OC(C)(C)C2O

InChI

InChIKey=RHSUJRQZTQNSLL-UHFFFAOYSA-N
InChI=1S/C12H15NO4/c1-12(2)10(14)7-5-4-6-8(9(7)17-12)16-11(15)13-3/h4-6,10,14H,1-3H3,(H,13,15)

HIDE SMILES / InChI

Molecular Formula C12H15NO4
Molecular Weight 237.2518
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Carbofuran and its toxic metabolites provide forensic evidence for furadan exposure in vultures (Gyps africanus) in Kenya.
2010-05
Soil and water contamination with carbofuran residues in agricultural farmlands in Kenya following the application of the technical formulation Furadan.
2010-02
Metabolism of carbosulfan. I. Species differences in the in vitro biotransformation by mammalian hepatic microsomes including human.
2009-10-07
Simultaneous determination of eight pesticide residues in coconut using MSPD and GC/MS.
2008-07-30
Hair analysis to document non-fatal pesticide intoxication cases.
2008-03-21
A physiologically based pharmacokinetic/pharmacodynamic model for carbofuran in Sprague-Dawley rats using the exposure-related dose estimating model.
2007-12
Liquid chromatography quadrupole time-of-flight mass spectrometry analysis of carbosulfan, carbofuran, 3-hydroxycarbofuran, and other metabolites in food.
2007-02-15
Survey of carbamate and organophosphorous pesticide export from a south Florida (U.S.A.) agricultural watershed: implications of sampling frequency on ecological risk estimation.
2006-11
Adsorption and degradation of benfuracarb in three soils in Hunan, People's Republic of China.
2006-04
Determination of carbosulfan and its metabolites in oranges by liquid chromatography ion-trap triple-stage mass spectrometry.
2006-03-24
Determination of pesticides in soy-based infant formula using liquid chromatography with electrospray ionization tandem mass spectrometry.
2006-03-04
Gas chromatographic-tandem mass spectrometric method for the quantitation of carbofuran, carbaryl and their main metabolites in applicators' urine.
2006-03-03
Comparison of four mass analyzers for determining carbosulfan and its metabolites in citrus by liquid chromatography/mass spectrometry.
2006
Determination of pesticides in apple-based infant foods using liquid chromatography electrospray ionization tandem mass spectrometry.
2005-02-09
A comparative study on the dissipation and microbial metabolism of organophosphate and carbamate insecticides in orchaqualf and fluvaquent soils of West Bengal.
2005-02
In vitro metabolism of carbofuran by human, mouse, and rat cytochrome P450 and interactions with chlorpyrifos, testosterone, and estradiol.
2004-12-07
Induction of carbofuran oxidation to 4-hydroxycarbofuran by Pseudomonas sp. 50432.
2002-09-10
Derivatization reactions of carbamate pesticides in supercritical carbon dioxide.
2002-09
Dermal pharmacokinetics of the insecticide furathiocarb in rats.
2002-01
Presence of carbamate pesticides in environmental waters from the northwest of Mexico: determination by liquid chromatography.
2001-06
Metabolism of carbofuran by Aspergillus niger and Fusarium graminearum.
1998-05
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:16:43 GMT 2025
Edited
by admin
on Mon Mar 31 22:16:43 GMT 2025
Record UNII
7J7N7A61BJ
Record Status Validated (UNII)
Record Version
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Name Type Language
3,7-BENZOFURANDIOL, 2,3-DIHYDRO-2,2-DIMETHYL-, 7-(METHYLCARBAMATE)
Preferred Name English
3-HYDROXYCARBOFURAN
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID2037506
Created by admin on Mon Mar 31 22:16:43 GMT 2025 , Edited by admin on Mon Mar 31 22:16:43 GMT 2025
PRIMARY
CAS
16655-82-6
Created by admin on Mon Mar 31 22:16:43 GMT 2025 , Edited by admin on Mon Mar 31 22:16:43 GMT 2025
PRIMARY
FDA UNII
7J7N7A61BJ
Created by admin on Mon Mar 31 22:16:43 GMT 2025 , Edited by admin on Mon Mar 31 22:16:43 GMT 2025
PRIMARY
PUBCHEM
27975
Created by admin on Mon Mar 31 22:16:43 GMT 2025 , Edited by admin on Mon Mar 31 22:16:43 GMT 2025
PRIMARY
Related Record Type Details
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