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Details

Stereochemistry ACHIRAL
Molecular Formula C7H8O
Molecular Weight 108.1378
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ANISOLE

SMILES

COC1=CC=CC=C1

InChI

InChIKey=RDOXTESZEPMUJZ-UHFFFAOYSA-N
InChI=1S/C7H8O/c1-8-7-5-3-2-4-6-7/h2-6H,1H3

HIDE SMILES / InChI

Molecular Formula C7H8O
Molecular Weight 108.1378
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Biradicals/zwitterions from thermolysis of enyne-isocyanates. Application to the synthesis of 2(1H)-pyridones, benzofuro[3,2-c]pyridin-1(2H)-ones, 2,5-dihydro-1H-pyrido[4,3-b]indol-1-ones, and related compounds.
2004-06-25
Transition metal-stabilized arenium cations: protonation of arenes dihapto-coordinated to pi-basic metal fragments.
2004-06-02
Characterization of rat liver microsomal metabolites of AM-630, a potent cannabinoid receptor antagonist, by high-performance liquid chromatography/electrospray ionization tandem mass spectrometry.
2004-06
Aryl cations from aromatic halides. Photogeneration and reactivity of 4-hydroxy(methoxy)phenyl cation.
2004-05-14
Cationic Rh complexes with novel spiro tetraarylpentaborate anions prepared from arylboronic acids and aryloxorhodium complexes.
2004-05-07
Potent and orally active ET(A) selective antagonists with 5,7-diarylcyclopenteno[1,2-b]pyridine-6-carboxylic acid structures.
2004-05-01
Pressure dependence of the dual luminescence of twisting molecules. The case of substituted 2,3-naphthalimides.
2004-05
Structure-activity comparison of YZ-069, a novel sigma ligand, and four analogs in receptor binding and behavioral studies.
2004-04
Structure-activity relationships of a novel class of endothelin receptor selective antagonists; 6-carboxy-2-isopropylamino-5,7-diarylcyclopenteno[1,2-b]pyridines.
2004-03-22
Stereoselective approach to C-aryl pyranoside synthesis which addresses the problem of C7-substitution in blepharocalyxin E.
2004-03-19
Synthesis, structural investigations and biological evaluation of novel hexahydropyridazine-1-carboximidamides, -carbothioamides and -carbothioimidic acid esters as inducible nitric oxide synthase inhibitors.
2004-03-01
Phenyl methyl ethers: novel electron donors for respiratory growth of Desulfitobacterium hafniense and Desulfitobacterium sp. strain PCE-S.
2004-03
Synthesis, structure, and magnetochemical analysis of selected first-row transition-metal anilino- and anisolesquarate compounds.
2004-02-09
Electron-transfer-induced substitution of alkylated C60 chlorides with proton sponge.
2004-01-23
An expeditious preparation of various sulfoforms of the disaccharide beta-D-Galp-(1-->3)-D-Galp, a partial structure of the linkage region of proteoglycans, as their 4-methoxyphenyl beta-D-glycosides.
2004-01-22
Synthesis and odour thresholds of mixed halogenated anisoles in water.
2004
Anisole, a new dopant for atmospheric pressure photoionization mass spectrometry of low proton affinity, low ionization energy compounds.
2004
Attempted syntheses of lanthanide(III) complexes of the anisole- and anilinosquarate ligands.
2003-12-15
Some aryl substituted 2-(4-nitrophenyl)-4-oxo-4-phenylbutanoates and 3-(4-nitrophenyl)-1-phenyl-1,4-butanediols and related compounds as inhibitors of rat liver microsomal retinoic acid metabolising enzymes.
2003-12
Addition of electron-rich aromatics to azafullerenium carbocation. A stepwise electrophilic substitution mechanism.
2003-11-27
Formation of gold-like metal-lustrous inclusion crystals from 1-phenyl-2,5-bis[5-(tricyanoethenyl)-2-thienyl]pyrrole host and an electron-donating aromatic guest.
2003-11-07
Acid-controlled photoreactions of aryl alkanoates: competition of transesterification, decarboxylation, Fries-rearrangement and/or transposition.
2003-11
Organolathanide-catalyzed regioselective intermolecular hydroamination of alkenes, alkynes, vinylarenes, di- and trivinylarenes, and methylenecyclopropanes. Scope and mechanistic comparison to intramolecular cyclohydroaminations.
2003-10-15
Structure-based design of novel guanidine/benzamidine mimics: potent and orally bioavailable factor Xa inhibitors as novel anticoagulants.
2003-10-09
Dynamic kinetic asymmetric cycloadditions of isocyanates to vinylaziridines.
2003-10-01
Unprecedented selective ipso-nitration of calixarenes monitored by the O-substituents.
2003-09-05
The use of imidazolium ionic liquids for the formation and stabilization of ir0 and rh0 nanoparticles: efficient catalysts for the hydrogenation of arenes.
2003-07-21
Structure-function relationships in high-density octadecylsilane stationary phases by Raman spectroscopy. 4. Effects of neutral and basic aromatic compounds.
2003-07-15
Acylation of aromatic ethers over solid acid catalysts: scope of the reaction with more complex acylating agents.
2003-07-07
In vivo study of the GC90/IRIV vaccine for immune response and autoimmunity into a novel humanised transgenic mouse.
2003-07-07
Two component model of orientationally ordered wall adjacent liquid layers.
2003-07-01
Sensitivity-enhanced phase-corrected ultra-slow magic angle turning using multiple-echo data acquisition.
2003-07
Non-polar halogenated natural products bioaccumulated in marine samples. II. Brominated and mixed halogenated compounds.
2003-07
Pharmacokinetic and tumour-photosensitizing properties of methoxyphenyl porphyrin derivative.
2003-06-24
A unique autocatalytic process and evidence for a concerted-stepwise mechanism transition in the dissociative electron-transfer reduction of aryl thiocyanates.
2003-06-18
The synthesis of carboacycles derived from B,B'-bis(aryl) derivatives of icosahedral ortho-carborane.
2003-06-16
Crystal structure of 3,3-dichloro-N-p-methoxyphenyl-4-(2-phenylstryl)-2-azetidinone.
2003-06
Structure-based approach to falcipain-2 inhibitors: synthesis and biological evaluation of 1,6,7-trisubstituted dihydroisoquinolines and isoquinolines.
2003-05-15
Novel preparation of 2,1-benzothiazine derivatives from sulfonamides with [hydroxy(tosyloxy)iodo]arenes.
2003-04-21
Novel nonimidazole histamine H3 receptor antagonists: 1-(4-(phenoxymethyl)benzyl)piperidines and related compounds.
2003-04-10
N-(4-Methoxybenzylidene)-N'-(2-pyridyl)hydrazine.
2003-04
An extremely facile aza-Bergman rearrangement of sterically unencumbered acyclic 3-aza-3-ene-1,5-diynes.
2003-03-21
Dimethyl 6-methoxy-4abeta-methyl-9-oxo-1,2,3,4,4a,9,10,10abeta-octahydrophenanthrene-1,1-dicarboxylate.
2003-03
(Arene)tricarbonylchromium complexes synthesized on NaX zeolite: solid-state NMR and DRIFTS studies.
2003-01-27
Synthesis of furo[3,4-c]furans using a rhodium(II)-catalyzed cyclization/Diels-Alder cycloaddition sequence.
2003-01-24
High resolution electronic absorption spectra of anisole and phenoxyl radical.
2003-01-01
Structure-affinity relationship study on N-[4-(4-arylpiperazin-1-yl)butyl]arylcarboxamides as potent and selective dopamine D(3) receptor ligands.
2002-12-19
Electron paramagnetic resonance backbone dynamics studies on spin-labelled neuropeptide Y analogues.
2002-12
Cycloheptyne intermediate in the reaction of chiral cyclohexylidenemethyliodonium salt with sulfonates.
2002-11-15
Synthesis, cytotoxicity and antitumor activity of 2,3-diarylcyclopent-2-ene-1-ones.
2002-10
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:55:27 GMT 2025
Edited
by admin
on Mon Mar 31 17:55:27 GMT 2025
Record UNII
B3W693GAZH
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FEMA NO. 2097
Preferred Name English
ANISOLE
FCC   FHFI   HSDB   MI   USP-RS  
Systematic Name English
ANISOLE [FCC]
Common Name English
ANISOLE [FHFI]
Common Name English
ANISOLE [USP-RS]
Common Name English
PHENYL METHYL ETHER
Systematic Name English
PHENOXYMETHANE
Systematic Name English
METHYLPHENYL ETHER
Systematic Name English
METHYL PHENYL ETHER
Systematic Name English
ETHER, METHYL PHENYL
Systematic Name English
NSC-7920
Code English
METHOXYBENZENE
Systematic Name English
BENZENE, METHOXY-
Systematic Name English
ANISOLE [HSDB]
Common Name English
ANISOLE [MI]
Common Name English
Classification Tree Code System Code
JECFA EVALUATION ANISOLE
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
Code System Code Type Description
CHEBI
16579
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
MERCK INDEX
m1932
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY Merck Index
RS_ITEM_NUM
1037011
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
CAS
100-66-3
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
DAILYMED
B3W693GAZH
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
EPA CompTox
DTXSID4041608
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
NSC
7920
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
HSDB
44
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
JECFA MONOGRAPH
1250
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
RXCUI
2594597
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-876-1
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
WIKIPEDIA
ANISOLE
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
FDA UNII
B3W693GAZH
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
CHEBI
51683
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
PUBCHEM
7519
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY