2-METHYLANISOLE

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 Search

SMILES

COC1=CC=CC=C1C

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

Molecular Formula	C8H10O
Molecular Weight	122.1644
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
Ligand effects in chromium diphosphine catalysed olefin co-trimerisation and diene trimerisation.	2010-01-14	20023994
Properties of the [M(dppm)2M']2+ building blocks (M, M' = Pd or Pt): site selectivity, emission features, and frontier orbital analysis.	2009-05-04	19348458
(+)- and (-)-mutisianthol: first total synthesis, absolute configuration, and antitumor activity.	2009-03-20	19231874
5-(2-Methoxy-benz-yl)-4-(2-methoxy-phen-yl)-4H-1,2,4-triazol-3-ol.	2009-01-17	21581933
Carbohydrate-derived 1,3-diphosphite ligands as chiral nanoparticle stabilizers: promising catalytic systems for asymmetric hydrogenation.	2009	19598200
Peptidomimetic inhibitors of farnesyltransferase with high in vitro activity and significant cellular potency.	2007-11-15	17889533
Insertion reactions of alkynes and organic isocyanides into the palladium-carbon bond of dimetallic Fe-Pd alkoxysilyl complexes.	2006-11-28	17088964
Rotationally resolved electronic spectra of 2- and 3-methylanisole in the gas phase: a study of methyl group internal rotation.	2006-10-12	17020377
Beta-aryl eliminations from Rh(I) iminyl complexes.	2005-08-24	16104735
Smooth muscle relaxant action of benzyl benzoates and salicylic acid derivatives from Brickellia veronicaefolia on isolated guinea-pig ileum.	2005-04	15856407
Scope and limitations of the nitro-Mannich reaction for the stereoselective synthesis of 1,2-diamines.	2005-01-21	15651800
Ligand bite governs enantioselectivity: electronic and steric control in Pd-catalyzed allylic alkylations by modular fenchyl phosphinites (FENOPs).	2004-10-25	15378682
Ag-catalyzed asymmetric mannich reactions of enol ethers with aryl, alkyl, alkenyl, and alkynyl imines.	2004-03-31	15038725
Highly enantiomerically enriched chlorophosphine boranes: synthesis and applications as P-chirogenic electrophilic blocks.	2003-05-30	12762729
Chemistry and immunomodulatory activity of frankincense oil.	2003-04-25	12710734
Novel N1-(benzyl)cinnamamidine derived NR2B subtype-selective NMDA receptor antagonists.	2003-02-24	12639560
An experimental and computational evaluation of the energetics of the isomeric methoxyphenylcarbenes generated in carbon atom reactions.	2002-01-16	11782188
Steric and electronic ligand perturbations in catalysis: asymmetric allylic substitution reactions using C2-symmetrical phosphorus-chiral (bi)ferrocenyl donors.	2001-02-09	11430094
Hexahydrochromeno[4,3-b]pyrrole derivatives as acetylcholinesterase inhibitors.	2001-01-04	11141093
An assessment of the reaction energetics for cytochrome P450-mediated reactions.	2001-01-01	11361021

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:19:11 GMT 2025` Edited by `admin` on `Mon Mar 31 19:19:11 GMT 2025`
Record UNII	09G73SL17K
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

FEMA NO. 2680

Preferred Name

English

2-METHYLANISOLE

Systematic Name

English

O-METHOXYTOLUENE

Common Name

English

NSC-6253

Code

English

ANISOLE, O-METHYL-

Common Name

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