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anisole

Structure via PubChem · Public domain (PubChem)

EntityQ312244· pop 35· linked from 65 articles

Also known as methoxybenzene, phenoxymethane, methyl phenyl ether, phenyl methyl ether

Anisole, or methoxybenzene, is an organic compound with the formula . It is a colorless liquid with a smell reminiscent of anise seed, and in fact many of its derivatives are found in natural and artificial fragrances. The compound is mainly made synthetically and is a precursor to other synthetic compounds. Structurally, it is an ether () with a methyl () and phenyl () group attached. Anisole is a standard reagent of both practical and pedagogical value.

Chemical data

Formula
C7H8O
Molecular weight
108.14 g/mol
IUPAC name
anisole
SMILES
COC1=CC=CC=C1
InChIKey
RDOXTESZEPMUJZ-UHFFFAOYSA-N
XLogP
2.1
Polar surface area
9.2 Ų
H-bond donors
0
H-bond acceptors
1
Formal charge
0

via PubChem

Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Has part
hydrogen
Mass
108.058
Autonomy
475
Show 20 more facts
found in taxon
Physarum polycephalum
Commons category
Anisole
refractive index
1.5174
canonical SMILES
COC1=CC=CC=C1
chemical formula
C₇H₈O
melting point
-37.3
boiling point
153.6
density
0.9940
partition coefficient water/octanol
2.11
phase point
critical point
electric dipole moment
1.38
flash point
41
vapor pressure
53.1
lower flammable limit
1.2
upper flammable limit
6.3
dynamic viscosity
0.427
surface tension
29.08
median lethal dose (LD50)
3.7
ionization energy
8.21
Sources (4)

via Wikidata · CC0

~3 min read

Encyclopedic overview

8 sections
Contents
  • Reactivity
  • Synthesis
  • Applications
  • Safety
  • Popular culture
  • See also
  • References
  • External links

Anisole, or methoxybenzene, is an organic compound with the formula . It is a colorless liquid with a smell reminiscent of anise seed, and in fact many of its derivatives are found in natural and artificial fragrances. The compound is mainly made synthetically and is a precursor to other synthetic compounds. Structurally, it is an ether () with a methyl () and phenyl () group attached. Anisole is a standard reagent of both practical and pedagogical value.

==Reactivity== Anisole undergoes electrophilic aromatic substitution reaction at a faster speed than benzene, which in turn reacts more quickly than nitrobenzene. The methoxy group is an ortho/para directing group, which means that electrophilic substitution preferentially occurs at these three sites. The enhanced nucleophilicity of anisole vs. benzene reflects the influence of the methoxy group, which renders the ring more electron-rich. The methoxy group strongly affects the pi cloud of the ring as a mesomeric electron donor, more so than as an inductive electron withdrawing group despite the electronegativity of the oxygen. Stated more quantitatively, the Hammett constant for para-substitution of anisole is –0.27.

Excerpted from Wikipedia’s “anisole” article, available under the CC BY-SA 4.0 licence.