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

Details

Stereochemistry ACHIRAL
Molecular Formula C8H10O
Molecular Weight 122.1644
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-METHYLANISOLE

SMILES

COC1=C(C)C=CC=C1

InChI

InChIKey=DTFKRVXLBCAIOZ-UHFFFAOYSA-N
InChI=1S/C8H10O/c1-7-5-3-4-6-8(7)9-2/h3-6H,1-2H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Hexahydrochromeno[4,3-b]pyrrole derivatives as acetylcholinesterase inhibitors.
2001 Jan 4
Novel N1-(benzyl)cinnamamidine derived NR2B subtype-selective NMDA receptor antagonists.
2003 Feb 24
Chemistry and immunomodulatory activity of frankincense oil.
2003 Mar-Apr
Highly enantiomerically enriched chlorophosphine boranes: synthesis and applications as P-chirogenic electrophilic blocks.
2003 May 30
Ag-catalyzed asymmetric mannich reactions of enol ethers with aryl, alkyl, alkenyl, and alkynyl imines.
2004 Mar 31
Ligand bite governs enantioselectivity: electronic and steric control in Pd-catalyzed allylic alkylations by modular fenchyl phosphinites (FENOPs).
2004 Oct 25
Smooth muscle relaxant action of benzyl benzoates and salicylic acid derivatives from Brickellia veronicaefolia on isolated guinea-pig ileum.
2005 Apr
Beta-aryl eliminations from Rh(I) iminyl complexes.
2005 Aug 24
Scope and limitations of the nitro-Mannich reaction for the stereoselective synthesis of 1,2-diamines.
2005 Jan 21
Insertion reactions of alkynes and organic isocyanides into the palladium-carbon bond of dimetallic Fe-Pd alkoxysilyl complexes.
2006 Nov 28
Rotationally resolved electronic spectra of 2- and 3-methylanisole in the gas phase: a study of methyl group internal rotation.
2006 Oct 12
Peptidomimetic inhibitors of farnesyltransferase with high in vitro activity and significant cellular potency.
2007 Nov 15
Carbohydrate-derived 1,3-diphosphite ligands as chiral nanoparticle stabilizers: promising catalytic systems for asymmetric hydrogenation.
2009
5-(2-Methoxy-benz-yl)-4-(2-methoxy-phen-yl)-4H-1,2,4-triazol-3-ol.
2009 Jan 17
(+)- and (-)-mutisianthol: first total synthesis, absolute configuration, and antitumor activity.
2009 Mar 20
Properties of the [M(dppm)2M']2+ building blocks (M, M' = Pd or Pt): site selectivity, emission features, and frontier orbital analysis.
2009 May 4
Ligand effects in chromium diphosphine catalysed olefin co-trimerisation and diene trimerisation.
2010 Jan 14
Patents
Name Type Language
2-METHYLANISOLE
Systematic Name English
O-METHOXYTOLUENE
Common Name English
NSC-6253
Code English
ANISOLE, O-METHYL-
Common Name English
FEMA NO. 2680
Code English
O-METHYL ANISOLE
Common Name English
O-CRESYL METHYL ETHER
Common Name English
BENZENE, 1-METHOXY-2-METHYL-
Systematic Name English
O-METHYLANISOLE [FHFI]
Common Name English
Classification Tree Code System Code
CFR 21 CFR 172.515
Created by admin on Fri Dec 15 18:43:26 GMT 2023 , Edited by admin on Fri Dec 15 18:43:26 GMT 2023
JECFA EVALUATION O-METHYLANISOLE
Created by admin on Fri Dec 15 18:43:26 GMT 2023 , Edited by admin on Fri Dec 15 18:43:26 GMT 2023
Code System Code Type Description
JECFA MONOGRAPH
1251
Created by admin on Fri Dec 15 18:43:26 GMT 2023 , Edited by admin on Fri Dec 15 18:43:26 GMT 2023
PRIMARY
NSC
6253
Created by admin on Fri Dec 15 18:43:26 GMT 2023 , Edited by admin on Fri Dec 15 18:43:26 GMT 2023
PRIMARY
MESH
C428434
Created by admin on Fri Dec 15 18:43:26 GMT 2023 , Edited by admin on Fri Dec 15 18:43:26 GMT 2023
PRIMARY
CHEBI
141702
Created by admin on Fri Dec 15 18:43:26 GMT 2023 , Edited by admin on Fri Dec 15 18:43:26 GMT 2023
PRIMARY
CAS
578-58-5
Created by admin on Fri Dec 15 18:43:26 GMT 2023 , Edited by admin on Fri Dec 15 18:43:26 GMT 2023
PRIMARY
EPA CompTox
DTXSID9060368
Created by admin on Fri Dec 15 18:43:26 GMT 2023 , Edited by admin on Fri Dec 15 18:43:26 GMT 2023
PRIMARY
ECHA (EC/EINECS)
209-426-3
Created by admin on Fri Dec 15 18:43:26 GMT 2023 , Edited by admin on Fri Dec 15 18:43:26 GMT 2023
PRIMARY
PUBCHEM
33637
Created by admin on Fri Dec 15 18:43:26 GMT 2023 , Edited by admin on Fri Dec 15 18:43:26 GMT 2023
PRIMARY
FDA UNII
09G73SL17K
Created by admin on Fri Dec 15 18:43:26 GMT 2023 , Edited by admin on Fri Dec 15 18:43:26 GMT 2023
PRIMARY