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149160

3-Methylanisole

Name: 3-Methylanisole
Brand: ALDRICH

99%

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About This Item

Linear Formula:

CH₃C₆H₄OCH₃

CAS Number:

100-84-5

Molecular Weight:

122.16

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24848934

EC Number:

202-893-4

Beilstein/REAXYS Number:

907023

MDL number:

MFCD00008395

Assay:

99%

Form:

liquid

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Properties

Quality Level

200

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

Description

Application

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

pictograms

GHS02,GHS07

signalword

Warning

hcodes

H226,H302

pcodes

P210 - P233 - P240 - P241 - P242 - P301 + P312

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk

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

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number

0000428382

0000411462

0000321988

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Expedient Route to the functionalized calyciphylline A-type skeleton via a Michael addition-RCM strategy.

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.

Global Trade Item Number

SKU	GTIN
149160-100ML	04061838738219