Skip to Content
Merck
CN

Key Documents

View All Documentation

345059

4-Fluoro-2-nitrophenol

99%

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
FC6H3(NO2)OH
CAS Number:
394-33-2
Molecular Weight:
157.10
NACRES:
NA.22
PubChem Substance ID:
24861290
UNSPSC Code:
12352100
MDL number:
MFCD00042528
Assay:
99%
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

assay

99%

mp

75-77 °C (lit.)

functional group

fluoro, nitro

SMILES string

Oc1ccc(F)cc1[N+]([O-])=O

InChI

1S/C6H4FNO3/c7-4-1-2-6(9)5(3-4)8(10)11/h1-3,9H

InChI key

ZHRLVDHMIJDWSS-UHFFFAOYSA-N

General description

4-Fluoro-2-nitrophenol is formed during iron(III) nitrate nonahydrate activated by tungstophosphoric acid cesium salt catalyzed nitration of 4-fluorophenol.

Application

4-Fluoro-2-nitrophenol may be used in the preparation of 5-fluoro-2-methoxyanilineand 5-fluoro-2-hydroxyaniline.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品

This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
19028BD
07909BD
18701EO
11601HO
04512BR

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

SOME SYNTHESES FROM p-FLUOROANISOLE.
BUU-HOI NP, et al.
The Journal of Organic Chemistry, 19(10), 1617-1621 (1954)
I M Rietjens et al.
European journal of biochemistry, 194(3), 945-954 (1990-12-27)
Pathways for biodehalogenation of fluorinated aniline derivatives were investigated. Microsomal NADPH-dependent dehalogenation of fluoroanilines was shown to proceed by three different reaction pathways. The first route appeared to result in monooxygenation at a fluorinated position and release of the fluorine
Catalytic effects of some Keggin-type heteropoly acids and polyoxometalates on selective nitration of phenols.
Amani K and Maleki F.
Journal of the Iranian Chemical Society, 4(2), 238-243 (2007)
View All Related Papers

Global Trade Item Number

SKUGTIN
345059-5G04061832279923
345059-25G04061832279916