Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

162310

Sigma-Aldrich

3-Fluoroanisole

99%

Sign Into View Organizational & Contract Pricing

Select a Size

25 G
$50.10

$50.10

Available to ship onApril 22, 2025Details

Request a Bulk Order
All Photos(1)

Select a Size

Change View
25 G
$50.10

About This Item

Linear Formula:
FC6H4OCH3
CAS Number:
456-49-5
Molecular Weight:
126.13
EC Number:
207-267-4
MDL number:
MFCD00000335
UNSPSC Code:
12352100
PubChem Substance ID:
24849977
NACRES:
NA.22

$50.10

Available to ship onApril 22, 2025Details

Request a Bulk Order

Quality Level

100

assay

99%

form

liquid

refractive index

n20/D 1.488 (lit.)

bp

158 °C/743 mmHg (lit.)

density

1.104 g/mL at 25 °C (lit.)

functional group

fluoro

SMILES string

COc1cccc(F)c1

InChI

1S/C7H7FO/c1-9-7-4-2-3-6(8)5-7/h2-5H,1H3

InChI key

MFJNOXOAIFNSBX-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

3-Fluoroanisole was used in the synthesis of 4-fluoro-5,6-dihydroxytryptamine[1]. It was also used in the synthesis of 3-fluoro- and 5-fluoronoradrenaline[2].

pictograms

Flame
GHS02

signalword

Warning

hcodes

H226

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

111.2 °F - closed cup

flash_point_c

44 °C - closed cup

ppe

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
STBL2583
STBK1618
STBG3490V
STBC7012V
STBB8828V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

M Kawase et al.
Journal of medicinal chemistry, 33(8), 2204-2211 (1990-08-01)
The 5,6-dihydroxytryptamine (5,6-DHT) derivatives 4-fluoro- and 7-fluoro-5,6-DHTs (26a,b) and 4,7-difluoro-5,6-DHT (26c) were synthesized from 3-fluoroanisole (1) and 1,4-difluoro-2,3-dimethoxybenzene (13), respectively. Efficient methods were developed for the conversion of 1 to 4-fluoro- and 7-fluoro-5,6-bis(benzyloxy)indoles (12a,b, respectively), and 13 to 4,7-difluoro-5,6-[( diphenylmethylene)dioxy]indole
Synthesis and EPR investigations of fluorocatecholamines.
Stegmann HB, et al.
Journal of the Chemical Society. Perkin Transactions 1, 2(3), 547-555 (1994)
Oriol Planas et al.
Science (New York, N.Y.), 367(6475), 313-317 (2020-01-18)
Bismuth catalysis has traditionally relied on the Lewis acidic properties of the element in a fixed oxidation state. In this paper, we report a series of bismuth complexes that can undergo oxidative addition, reductive elimination, and transmetallation in a manner

Questions

Reviews

No rating value

Active Filters

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