Skip to Content
Merck
CN

196576

4-Nitro-2-(trifluoromethyl)aniline

98%

Synonym(s):

2-Amino-5-nitrobenzotrifluoride, 4-Nitro-α,α,α-trifluoro-o-toluidine

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
O2NC6H3(CF3)NH2
CAS Number:
Molecular Weight:
206.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-443-2
Beilstein/REAXYS Number:
2121347
MDL number:
Assay:
98%
Form:
powder
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

Product Name

4-Nitro-2-(trifluoromethyl)aniline, 98%

InChI key

HOTZLWVITTVZGY-UHFFFAOYSA-N

InChI

1S/C7H5F3N2O2/c8-7(9,10)5-3-4(12(13)14)1-2-6(5)11/h1-3H,11H2

SMILES string

Nc1ccc(cc1C(F)(F)F)[N+]([O-])=O

assay

98%

form

powder

mp

90-92 °C (lit.)

functional group

fluoro
nitro

Looking for similar products? Visit Product Comparison Guide

Application

4-Nitro-2-(trifluoromethyl)aniline was used in the synthesis of monoazo dyes.

General description

4-Nitro-2-(trifluoromethyl)aniline undergoes diazotization and coupling with:
  • N-hydroxyalkylamino-5-napthols
  • pyrazolones and naptholsulphonic acids
  • N-(2-cyanoethyl)-N-(hydroxyalkyl)anilines

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

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

Effect of fluorine substitution on color and fastness of monoazo dyes.
Dickey JB, et al.
Ind. and Eng. Chem., 45(8), 1730-1734 (1953)

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