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148091

Sigma-Aldrich

4-Methylanisole

99%

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About This Item

Linear Formula:
CH3C6H4OCH3
CAS Number:
104-93-8
Molecular Weight:
122.16
Beilstein/REAXYS Number:
1237336
EC Number:
203-253-7
MDL number:
MFCD00008413
UNSPSC Code:
12352100
PubChem Substance ID:
24848881
NACRES:
NA.22

vapor pressure

5.25 mmHg ( 50 °C)

assay

99%

form

liquid

refractive index

n20/D 1.511 (lit.)

bp

174 °C (lit.)

density

0.969 g/mL at 25 °C (lit.)

SMILES string

COc1ccc(C)cc1

InChI

1S/C8H10O/c1-7-3-5-8(9-2)6-4-7/h3-6H,1-2H3

InChI key

CHLICZRVGGXEOD-UHFFFAOYSA-N

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Application

4-Methylanisole was used to prepare 5-methoxy-1,8-dimethyltetralin. It was also used as the solubilizate molecule to study the site of incorporation of solubilizates in sodium dodecyl sulfate (SDS) micellar systems.

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Warning

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 3 - Repr. 2 - Skin Irrit. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

138.2 °F - closed cup

flash_point_c

59 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Brant L Kedrowski et al.
The Journal of organic chemistry, 73(13), 5177-5179 (2008-05-30)
A simple synthesis of the natural product cacalol has been developed that proceeds in seven steps and 21-25% overall yield. Ortho-lithiation of 4-methylanisole and alkylation with 5-iodo-1-pentene, followed by intramolecular Friedel-Crafts alkylation, gave 5-methoxy-1,8-dimethyltetralin. This compound was then formylated in
Suratkar et al.
Journal of colloid and interface science, 225(1), 32-38 (2000-04-18)
The site of incorporation of solubilizates in sodium dodecyl sulfate (SDS) micellar systems has been investigated by proton NMR spectroscopy. The solubilizate molecules chosen for the present study are phenol, 4-methylphenol, 4-allyl-2-methoxyphenol, anisole, 4-methylanisole, 4-propenylanisole, 1,8-cineole, and limonene. These molecules
Occurrence of aromatic methyl migration (NIH-shift) during oxidation of p-methylanisole by hemin-thiolester complex as a cytochrome P-450 model.
H Sakurai et al.
Biochemical and biophysical research communications, 108(4), 1649-1654 (1982-10-29)
B Brunsborg et al.
Toxicology letters, 73(3), 209-212 (1994-09-01)
4-Methoxytoluene was given by gavage to 4 groups of 20 rats at dosage levels of 0, 40, 120 or 240 mg kg-1 body weight/day for 4 weeks. There was a statistically significant decrease in serum creatinine and urea in the
Alessandro Scarso et al.
Journal of the American Chemical Society, 125(46), 13981-13983 (2003-11-13)
Reversible coencapsulation of a solute molecule and a single solvent molecule takes place in solution at ambient temperature. Two isomeric complexes are formed (social isomers), and their relative energies are assessed by NMR methods. Intermolecular interactions between 3 aromatic solutes
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