Skip to Content
MilliporeSigma
All Photos(2)

Documents

149160

Sigma-Aldrich

3-Methylanisole

99%

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
CH3C6H4OCH3
CAS Number:
100-84-5
Molecular Weight:
122.16
Beilstein/REAXYS Number:
907023
EC Number:
202-893-4
MDL number:
MFCD00008395
UNSPSC Code:
12352100
PubChem Substance ID:
24848934
NACRES:
NA.22

assay

99%

form

liquid

refractive index

n20/D 1.513 (lit.)

bp

175-176 °C (lit.)

density

0.969 g/mL at 25 °C (lit.)

SMILES string

COc1cccc(C)c1

InChI

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

InChI key

OSIGJGFTADMDOB-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

3-Methylanisole was used to study the functionalized core of calyciphylline A-type alkaloids.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

125.6 °F - closed cup

flash_point_c

52 °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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 6

1 of 6

1,3-Dimethoxybenzene ≥98%, FG

Sigma-Aldrich

W238503

1,3-Dimethoxybenzene

2′-Methylacetophenone 98%

Sigma-Aldrich

M26593

2′-Methylacetophenone

2,4,6-Trimethylphenol 97%

Sigma-Aldrich

T79006

2,4,6-Trimethylphenol

1,2,3-Trimethoxybenzene 98%

Sigma-Aldrich

137995

1,2,3-Trimethoxybenzene

4-Ethynylanisole 97%

Sigma-Aldrich

206490

4-Ethynylanisole

3-Methoxybenzyl bromide 98%

Sigma-Aldrich

429120

3-Methoxybenzyl bromide

Filippo Sladojevich et al.
Organic letters, 13(19), 5132-5135 (2011-09-09)
An efficient, robust, and scalable strategy to access the functionalized core of calyciphylline A-type alkaloids has been developed starting from commercially available 3-methylanisole. Key features of this approach are an intramolecular Michael addition/allylation sequence and a ring-closing metathesis step.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service