Skip to Content
Merck
CN

527653

2-Fluoro-5-nitrobenzyl alcohol

96%

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
FC6H3(NO2)CH2OH
CAS Number:
Molecular Weight:
171.13
UNSPSC Code:
12352100
PubChem Substance ID:
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

assay

96%

mp

68-71 °C (lit.)

SMILES string

OCc1cc(ccc1F)[N+]([O-])=O

InChI

1S/C7H6FNO3/c8-7-2-1-6(9(11)12)3-5(7)4-10/h1-3,10H,4H2

InChI key

IFIOUOYJVOSTFH-UHFFFAOYSA-N

General description

2-Fluoro-5-nitrobenzyl alcohol can be prepared from 2-fluoro-5-nitrobenzaldehyde.

Application

2-Fluoro-5-nitrobenzyl alcohol may be used to synthesize 2-fluoro-5-nitrobenzyl bromide and 5-amino-2-fluorobenzyl alcohol.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

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.

Already Own This Product?

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

Visit the Document Library

Ana Carolina Corrêa de Sousa et al.
Chemical & pharmaceutical bulletin, 64(6), 594-601 (2016-06-03)
Malaria is one of the most important tropical diseases; the use of amodiaquine as a current chemotherapy in the treatment of malaria has shown some problems such as hepatotoxicity and agranulocytosis. In this work we present the rational design, synthesis
4H-1-Benzopyrans by a tandem SN2-SNAr reaction.
Bunce RA, et al.
Journal of Heterocyclic Chemistry, 45(2), 547- 550 (2008)

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