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Details

Stereochemistry ACHIRAL
Molecular Formula C8H10O2
Molecular Weight 138.1638
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ANISYL ALCOHOL

SMILES

COC1=CC=C(CO)C=C1

InChI

InChIKey=MSHFRERJPWKJFX-UHFFFAOYSA-N
InChI=1S/C8H10O2/c1-10-8-4-2-7(6-9)3-5-8/h2-5,9H,6H2,1H3

HIDE SMILES / InChI

Molecular Formula C8H10O2
Molecular Weight 138.1638
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Chemical composition and antibacterial activities of Illicium verum against antibiotic-resistant pathogens.
2010-10
Determination of suspected allergens in cosmetic products by headspace-programmed temperature vaporization-fast gas chromatography-quadrupole mass spectrometry.
2010-07
Quantitative determination of some volatile suspected allergens in cosmetic creams spread on skin by direct contact sorptive tape extraction-gas chromatography-mass spectrometry.
2010-04-16
Potent new small-molecule inhibitor of botulinum neurotoxin serotype A endopeptidase developed by synthesis-based computer-aided molecular design.
2009-11-10
Aryl-alcohol oxidase involved in lignin degradation: a mechanistic study based on steady and pre-steady state kinetics and primary and solvent isotope effects with two alcohol substrates.
2009-09-11
Home-prepared anatase, rutile, and brookite TiO(2) for selective photocatalytic oxidation of 4-methoxybenzyl alcohol in water: reactivity and ATR-FTIR study.
2009-05
Green procedure for the preparation of scented alcohols from carbonyl compounds.
2008-04
Anomalous reactivity of radical cations produced by photosensitized oxidation of 4-methoxybenzyl alcohol derivatives: role of the sensitizer.
2008-01-07
Oxidation of aromatic alcohols in irradiated aqueous suspensions of commercial and home-prepared rutile TiO(2): a selectivity study.
2008
Thiourea-enhanced flavin photooxidation of benzyl alcohol.
2008
Synthesis and biological evaluation of phosphate prodrugs of 4-phospho-D-erythronohydroxamic acid, an inhibitor of 6-phosphogluconate dehydrogenase.
2007-08
High-performance liquid chromatographic method for the simultaneous determination of 24 fragrance allergens to study scented products.
2007-07-27
Sensitization to 26 fragrances to be labelled according to current European regulation. Results of the IVDK and review of the literature.
2007-07
Synthesis of 3'-deoxynucleosides with 2-oxabicyclo[3.1.0]hexane sugar moieties: addition of difluorocarbene to a 3',4'-unsaturated uridine derivative and 1,2-dihydrofurans derived from D- and L-xylose1.
2007-04-27
Direct detection of reactive nitrogen species in experimental autoimmune uveitis.
2007-03
Characterization of the amino acid adducts of the enedial derivative of teucrin A.
2006-10
Novel polyphenol oxidase mined from a metagenome expression library of bovine rumen: biochemical properties, structural analysis, and phylogenetic relationships.
2006-08-11
Effect of water on the functionalization of substituted anisoles with iodine in the presence of F-TEDA-BF4 or hydrogen peroxide.
2006-02-03
Enhancement of chain amplification in photoreactions of N-methoxypyridinium salts with alcohols.
2005-09-24
Spectral and catalytic properties of aryl-alcohol oxidase, a fungal flavoenzyme acting on polyunsaturated alcohols.
2005-08-01
A methoxy derivative of resveratrol analogue selectively induced activation of the mitochondrial apoptotic pathway in transformed fibroblasts.
2005-02-14
Catalytic photooxidation of 4-methoxybenzyl alcohol with a flavin-zinc(II)-cyclen complex.
2004-12-03
Biotransformations of propenylbenzenes by an Arthrobacter sp. and its t-anethole blocked mutants.
2003-10-09
First evidence of catalytic mediation by phenolic compounds in the laccase-induced oxidation of lignin models.
2003-09
Synthesis of orthogonally protected (R)- and (S)-2-methylcysteine via an enzymatic desymmeterization and Curtius rearrangement.
2003-06-27
One electron oxidation of benzyltrialkylsilanes catalysed by lignin peroxidase: comparison with the oxidation induced by chemical oxidants.
2003-04-04
Antioxidant activity and characterization of volatile constituents of Taheebo (Tabebuia impetiginosa Martius ex DC).
2003-01-01
Solid phase synthesis of hydrophobic difficult sequence peptides on BDDMA-PS support.
2001-12
Prochiral selectivity in H(2)O(2)-promoted oxidation of arylalkanols catalysed by chloroperoxidase. The role of the interactions between the OH group and the amino-acid residues in the enzyme active site.
2001-02
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:46:19 GMT 2025
Edited
by admin
on Mon Mar 31 18:46:19 GMT 2025
Record UNII
7N6XGV3U49
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ANISE ALCOHOL
INCI   MI  
INCI  
Preferred Name English
ANISYL ALCOHOL
FCC   FHFI  
Systematic Name English
4-METHOXYBENZYL ALCOHOL
Systematic Name English
BENZENEMETHANOL, 4-METHOXY-
Systematic Name English
ANISYL ALCOHOL [FHFI]
Common Name English
4-METHOXYBENZENEMETHANOL
Systematic Name English
ANISE ALCOHOL [MI]
Common Name English
PARA METHOXYBENZYL ALCOHOL
Systematic Name English
FEMA NO. 2099
Code English
(4-(METHYLOXY)PHENYL)METHANOL
Systematic Name English
ANISIC ALCOHOL
Common Name English
(4-METHOXYPHENYL)METHANOL
Systematic Name English
NSC-2151
Code English
P-METHOXYBENZYL ALCOHOL
Common Name English
BENZYL ALCOHOL, P-METHOXY-
Common Name English
ANISYL ALCOHOL [FCC]
Common Name English
Classification Tree Code System Code
JECFA EVALUATION ANISYL ALCOHOL
Created by admin on Mon Mar 31 18:46:19 GMT 2025 , Edited by admin on Mon Mar 31 18:46:19 GMT 2025
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 18:46:19 GMT 2025 , Edited by admin on Mon Mar 31 18:46:19 GMT 2025
EC SCIENTIFIC COMMITTEE ON CONSUMER SAFETY OPINION SCCS/1459/11
Created by admin on Mon Mar 31 18:46:19 GMT 2025 , Edited by admin on Mon Mar 31 18:46:19 GMT 2025
Code System Code Type Description
DAILYMED
7N6XGV3U49
Created by admin on Mon Mar 31 18:46:19 GMT 2025 , Edited by admin on Mon Mar 31 18:46:19 GMT 2025
PRIMARY
SMS_ID
100000159596
Created by admin on Mon Mar 31 18:46:19 GMT 2025 , Edited by admin on Mon Mar 31 18:46:19 GMT 2025
PRIMARY
EVMPD
SUB169887
Created by admin on Mon Mar 31 18:46:19 GMT 2025 , Edited by admin on Mon Mar 31 18:46:19 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-273-6
Created by admin on Mon Mar 31 18:46:19 GMT 2025 , Edited by admin on Mon Mar 31 18:46:19 GMT 2025
PRIMARY
WIKIPEDIA
Anisyl alcohol
Created by admin on Mon Mar 31 18:46:19 GMT 2025 , Edited by admin on Mon Mar 31 18:46:19 GMT 2025
PRIMARY
RXCUI
1424668
Created by admin on Mon Mar 31 18:46:19 GMT 2025 , Edited by admin on Mon Mar 31 18:46:19 GMT 2025
PRIMARY RxNorm
PUBCHEM
7738
Created by admin on Mon Mar 31 18:46:19 GMT 2025 , Edited by admin on Mon Mar 31 18:46:19 GMT 2025
PRIMARY
CAS
105-13-5
Created by admin on Mon Mar 31 18:46:19 GMT 2025 , Edited by admin on Mon Mar 31 18:46:19 GMT 2025
PRIMARY
MERCK INDEX
m1928
Created by admin on Mon Mar 31 18:46:19 GMT 2025 , Edited by admin on Mon Mar 31 18:46:19 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID6044357
Created by admin on Mon Mar 31 18:46:19 GMT 2025 , Edited by admin on Mon Mar 31 18:46:19 GMT 2025
PRIMARY
MESH
C066943
Created by admin on Mon Mar 31 18:46:19 GMT 2025 , Edited by admin on Mon Mar 31 18:46:19 GMT 2025
PRIMARY
FDA UNII
7N6XGV3U49
Created by admin on Mon Mar 31 18:46:19 GMT 2025 , Edited by admin on Mon Mar 31 18:46:19 GMT 2025
PRIMARY
NSC
2151
Created by admin on Mon Mar 31 18:46:19 GMT 2025 , Edited by admin on Mon Mar 31 18:46:19 GMT 2025
PRIMARY
JECFA MONOGRAPH
737
Created by admin on Mon Mar 31 18:46:19 GMT 2025 , Edited by admin on Mon Mar 31 18:46:19 GMT 2025
PRIMARY