U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C11H16N2O2
Molecular Weight 208.2569
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AMINOCARB

SMILES

CNC(=O)OC1=CC(C)=C(C=C1)N(C)C

InChI

InChIKey=IMIDOCRTMDIQIJ-UHFFFAOYSA-N
InChI=1S/C11H16N2O2/c1-8-7-9(15-11(14)12-2)5-6-10(8)13(3)4/h5-7H,1-4H3,(H,12,14)

HIDE SMILES / InChI

Molecular Formula C11H16N2O2
Molecular Weight 208.2569
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Comparison of the activity of topically applied pesticides and the herbicide 2,4-D in two short-term in vivo assays of genotoxicity in the mouse.
1990 Nov
Photolysis of pesticides: influence of epicuticular waxes from Persica laevis DC on the photodegradation in the solid phase of aminocarb, methiocarb and fenthion.
2001 Jun
[Lipoxygenase-mediated N-demethylation of pesticides in vitro].
2002 Dec
Immunomodulatory effect of various anti-parasitics: a review.
2006 Mar
Application of chemometrics methods for the simultaneous kinetic spectrophotometric determination of aminocarb and carbaryl in vegetable and water samples.
2009 Sep 15
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:53:06 GMT 2023
Edited
by admin
on Fri Dec 15 17:53:06 GMT 2023
Record UNII
767M03K32Y
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AMINOCARB
HSDB   ISO   MI  
Common Name English
4-(DIMETHYLAMINO)-3-METHYLPHENYL N-METHYLCARBAMATE
Systematic Name English
AMINOCARB [HSDB]
Common Name English
AMINOCARB [ISO]
Common Name English
AMINOCARB [MI]
Common Name English
4-DIMETHYLAMINO-M-TOLYL METHYLCARBAMATE
Systematic Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 44401
Created by admin on Fri Dec 15 17:53:06 GMT 2023 , Edited by admin on Fri Dec 15 17:53:06 GMT 2023
Code System Code Type Description
WIKIPEDIA
AMINOCARB
Created by admin on Fri Dec 15 17:53:06 GMT 2023 , Edited by admin on Fri Dec 15 17:53:06 GMT 2023
PRIMARY
MESH
C006511
Created by admin on Fri Dec 15 17:53:06 GMT 2023 , Edited by admin on Fri Dec 15 17:53:06 GMT 2023
PRIMARY
CAS
2032-59-9
Created by admin on Fri Dec 15 17:53:06 GMT 2023 , Edited by admin on Fri Dec 15 17:53:06 GMT 2023
PRIMARY
ALANWOOD
aminocarb
Created by admin on Fri Dec 15 17:53:06 GMT 2023 , Edited by admin on Fri Dec 15 17:53:06 GMT 2023
PRIMARY
CHEBI
2653
Created by admin on Fri Dec 15 17:53:06 GMT 2023 , Edited by admin on Fri Dec 15 17:53:06 GMT 2023
PRIMARY
EPA CompTox
DTXSID7022172
Created by admin on Fri Dec 15 17:53:06 GMT 2023 , Edited by admin on Fri Dec 15 17:53:06 GMT 2023
PRIMARY
MERCK INDEX
m1698
Created by admin on Fri Dec 15 17:53:06 GMT 2023 , Edited by admin on Fri Dec 15 17:53:06 GMT 2023
PRIMARY Merck Index
FDA UNII
767M03K32Y
Created by admin on Fri Dec 15 17:53:06 GMT 2023 , Edited by admin on Fri Dec 15 17:53:06 GMT 2023
PRIMARY
HSDB
561
Created by admin on Fri Dec 15 17:53:06 GMT 2023 , Edited by admin on Fri Dec 15 17:53:06 GMT 2023
PRIMARY
ECHA (EC/EINECS)
217-990-7
Created by admin on Fri Dec 15 17:53:06 GMT 2023 , Edited by admin on Fri Dec 15 17:53:06 GMT 2023
PRIMARY
NCI_THESAURUS
C163585
Created by admin on Fri Dec 15 17:53:06 GMT 2023 , Edited by admin on Fri Dec 15 17:53:06 GMT 2023
PRIMARY
PUBCHEM
16247
Created by admin on Fri Dec 15 17:53:06 GMT 2023 , Edited by admin on Fri Dec 15 17:53:06 GMT 2023
PRIMARY