Skip to Content
Merck
CN

348228

3-(Trifluoromethyl)phenylhydrazine

technical grade, 90%

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
CF3C6H4NHNH2
CAS Number:
Molecular Weight:
176.14
UNSPSC Code:
12352100
PubChem Substance ID:
EC Number:
206-713-5
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

InChI key

RSESUCWJKLHXEZ-UHFFFAOYSA-N

InChI

1S/C7H7F3N2/c8-7(9,10)5-2-1-3-6(4-5)12-11/h1-4,12H,11H2

SMILES string

NNc1cccc(c1)C(F)(F)F

grade

technical grade

assay

90%

refractive index

n20/D 1.504 (lit.)

bp

80-83 °C/9 mmHg (lit.)

density

1.348 g/mL at 25 °C (lit.)

General description

3-(Trifluoromethyl)phenylhydrazine can be prepared by reduction of 3-(trifluoromethyl)phenyldiazonium chloride.

Application

3-(Trifluoromethyl)phenylhydrazine may be used in the synthesis of N-2-diphenylhydrazinecarboxamides and N-2-diphenylhydrazine carbothioamides, having antitubercular and fungicidal activity.

pictograms

Exclamation mark

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

10 - Combustible liquids

wgk

WGK 3

flash_point_f

224.6 °F - closed cup

flash_point_c

107 °C - closed cup

ppe

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

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

Synthesis of new fluorine substituted hydrazinecarboxamides and hydrazine carbothioamides having antitubercular and fungicidal activity
Nalavde YM and Joshi V.
Indian J. Chem. B, 39(8), 634-637 (2000)

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