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

Details

Stereochemistry ACHIRAL
Molecular Formula C7H7NO2
Molecular Weight 137.136
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARBANILIC ACID

SMILES

OC(=O)NC1=CC=CC=C1

InChI

InChIKey=PWXJULSLLONQHY-UHFFFAOYSA-N
InChI=1S/C7H7NO2/c9-7(10)8-6-4-2-1-3-5-6/h1-5,8H,(H,9,10)

HIDE SMILES / InChI

Molecular Formula C7H7NO2
Molecular Weight 137.136
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Human OGA binds substrates in a conserved peptide recognition groove.
2010-11-15
Long-acting anticholinesterases for myasthenia gravis: synthesis and activities of quaternary phenylcarbamates of neostigmine, pyridostigmine and physostigmine.
2010-07-01
Palladium-catalyzed ortho-arylation of O-phenylcarbamates with simple arenes and sodium persulfate.
2010-04-28
Synthesis and chiral recognition of novel amylose derivatives containing regioselectively benzoate and phenylcarbamate groups.
2010-02-12
2-Carboxy-anilinium bromide monohydrate.
2009-11-28
Cholest-5-en-3β-yl N-phenyl-carbamate.
2009-11-28
Bis(3-carboxy-anilinum) bis-(perchlorate) monohydrate.
2009-07-04
Nested PCR-RFLP is a high-speed method to detect fungicide-resistant Botrytis cinerea at an early growth stage of grapes.
2009-02
Molecular structure and liquid-crystalline characteristics of chitosan phenylcarbamate.
2009-01-12
The old and new therapeutic approaches to the treatment of giardiasis: where are we?
2009
Immobilization of cellulose phenylcarbamate onto silica gel via in termolecular polycondensation of triethoxysilyl groups introduced with (3-glycidoxypropyl)triethoxysilane.
2008-10
The oxidation products of melatonin derivatives exhibit acetylcholinesterase and butyrylcholinesterase inhibitory activity.
2008-08
[Synthesis of 2-{3-[4-(4-fluorophenyl)-1-piperazinyl]-2-hydroxy-propoxy}-phenylcarbamic acid alkylesters and in vitro evaluation of their beta-antiadrenergic and vasodilatative activities].
2008-06
Enantioseparation using urea- and imide-bearing chitosan phenylcarbamate derivatives as chiral stationary phases for high-performance liquid chromatography.
2008-03
Molecular characterization of benzimidazole-resistant isolates of Cladosporium fulvum.
2008-01
Carbanilation of cereal beta-glucans for molecular weight determination and conformational studies.
2007-08-13
Preparation and chromatographic properties of a multimodal chiral stationary phase based on phenyl-carbamate-propyl-beta-CD for HPLC.
2007-08
[Study on enantioselectivity of celluloses derived by phenylcarbamate at 2,3- or 2,3,6-positions].
2007-03
[Potentiometric determination of aqueous dissociation constants of 2-,3-,4-{3-(4-benzhydryl-piperazine-1-yl)-2-hydroxy-propoxy}-phenylcarbamic acid alkylesters, water insoluble potential blockers of beta-adrenergic receptors].
2006-11
Is there a place for local anesthetics structurally different from classical amid or ester local anesthetics?
2006-10
High-performance liquid chromatographic enantioseparations on capillary columns containing crosslinked polysaccharide phenylcarbamate derivatives attached to monolithic silica.
2006-08
The use of artificial neural networks for the selection of the most appropriate thermal parameters and for the classification of a set of phenylcarbamic acid derivates.
2006-07
Carbonic anhydrase inhibitors: X-ray and molecular modeling study for the interaction of a fluorescent antitumor sulfonamide with isozyme II and IX.
2006-06-28
Change of the persistence lengths in the conformational transitions of pullulan- and amylose-tricarbanilates.
2006-05-20
Enantioselective LC/MS method for the determination of an antimalarial agent Fenozan B07 in dog plasma.
2006-05-15
2,4-Dimethoxyphenylsemicarbazones with anticonvulsant activity against three animal models of seizures: synthesis and pharmacological evaluation.
2006-05-01
[Analysis of reproductive development of mutant Nicotiana sylvestris plants resistant to isopropyl-N-phenylcarbamate].
2006-01-07
[HPLC separation of racemic basic esters of alkoxyphenylcarbamic acid using two teicoplanin chiral stationary phases].
2005-07
Phenserine Axonyx.
2005-07
An overview of phenserine tartrate, a novel acetylcholinesterase inhibitor for the treatment of Alzheimer's disease.
2005-07
Samarium diiodide promoted generation and asymmetric hydroxyalkylation of N,O-diprotected (3S)-3-pyrrolidinol 2-carbanions.
2005-02-17
[Adsorption of substances on active charcoal. Part 2: basic esters of phenylcarbamic acid with beta-adrenolytic effect].
2005-01
[Adsorption of substances on active charcoal. Part 1: Basic esters of phenylcarbamic acid with local anaesthetic effect].
2004-11
Synthesis and evaluation of phenylcarbamate derivatives as ligands for nicotinic acetylcholine receptors.
2004-09-15
Study of the mechanism of enantioseparation part VI: thermodynamic study of HPLC separation of some enantiomers of phenylcarbamic acid derivatives on a (S,S) Whelk-O 1 column.
2004-08
Synthesis of new OBAN's and further studies on positioning of the catalytic group.
2004-07-07
[Separation of enantiomers of phenylcarbamic acid derivatives by HPLC method].
2004-07
Biomolecule-compatible support structures for biomolecule coupling to physical measuring principle surfaces.
2004-06
In vitro activity of two phenyl-carbamate derivatives, singly and in combination with albendazole against albendazole-resistant Giardia intestinalis.
2004-05-07
Synthesis of chiral stationary phases with radical polymerization reaction of cellulose phenylcarbamate derivatives and vinylized silica gel.
2004-04-23
[Induction and genetic analysis of laboratory mutants of Gibberella zeae resistance to carbendazim].
2004-04
Selectivity tuning of serially coupled (S,S) Whelk-O 1 and (R,R) Whelk-O 1 columns in HPLC.
2004-03
A new group of potential antituberculotics: hydrochlorides of piperidinylalkyl esters of alkoxy-substituted phenylcarbamic acids.
2004
Chiral separation by HPLC using polysaccharide-based chiral stationary phases.
2004
Kinetic study of derivatives of phenylcarbamic acid enantiomers in rabbit blood serum using an on-line coupled column liquid chromatographic system.
2003-07
[Effect of saccharides in the teicoplanin stationary phase on the separation of enantiomers of the phenylcarbamic type using HPLC].
2003-03
Study of local anaesthetics, part 161: Influence of additives upon the release of a potential drug of a group of esters of phenylcarbamic acids from a hydroxyethyl cellulose hydrogel.
2003-02
Coupled column chromatography for separation and determination of enantiomers of phenylcarbamic acid derivatives in serum.
2003-02
Antimycobacterial activity of piperidinylpropyl esters of alkoxy-substituted phenylcarbamic acids.
2003
Antimycobacterial activity of basic ethyl esters of alkoxy-substituted phenylcarbamic acids.
2003
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:05:45 GMT 2025
Edited
by admin
on Mon Mar 31 19:05:45 GMT 2025
Record UNII
M19U56546G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CARBANILIC ACID [MI]
Preferred Name English
CARBANILIC ACID
MI  
Common Name English
N-PHENYLCARBAMIC ACID
Systematic Name English
PHENYLCARBAMIC ACID
Systematic Name English
N-CARBOXYANILINE
Systematic Name English
Code System Code Type Description
MESH
C059692
Created by admin on Mon Mar 31 19:05:45 GMT 2025 , Edited by admin on Mon Mar 31 19:05:45 GMT 2025
PRIMARY
CHEBI
52496
Created by admin on Mon Mar 31 19:05:45 GMT 2025 , Edited by admin on Mon Mar 31 19:05:45 GMT 2025
PRIMARY
PUBCHEM
10392
Created by admin on Mon Mar 31 19:05:45 GMT 2025 , Edited by admin on Mon Mar 31 19:05:45 GMT 2025
PRIMARY
CAS
501-82-6
Created by admin on Mon Mar 31 19:05:45 GMT 2025 , Edited by admin on Mon Mar 31 19:05:45 GMT 2025
PRIMARY
MERCK INDEX
m1054
Created by admin on Mon Mar 31 19:05:45 GMT 2025 , Edited by admin on Mon Mar 31 19:05:45 GMT 2025
PRIMARY Merck Index
FDA UNII
M19U56546G
Created by admin on Mon Mar 31 19:05:45 GMT 2025 , Edited by admin on Mon Mar 31 19:05:45 GMT 2025
PRIMARY