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p-trifluoromethylphenylhydrazine

Names

[ CAS No. ]:
368-90-1

[ Name ]:
p-trifluoromethylphenylhydrazine

[Synonym ]:
Hydrazine, [4-(trifluoromethyl)phenyl]-
(4-(Trifluoromethyl)phenyl)hydrazine
p-trifluoromethylphenylhydrazine
[4-(Trifluoromethyl)phenyl]hydrazine
MFCD00042508
4-(Trifluoromethyl)phenylhydrazine

Chemical & Physical Properties

[ Density]:
1.4±0.1 g/cm3

[ Boiling Point ]:
230.0±40.0 °C at 760 mmHg

[ Melting Point ]:
63-65 °C(lit.)

[ Molecular Formula ]:
C7H7F3N2

[ Molecular Weight ]:
176.139

[ Flash Point ]:
92.9±27.3 °C

[ Exact Mass ]:
176.056137

[ PSA ]:
38.05000

[ LogP ]:
2.26

[ Vapour Pressure ]:
0.1±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.526

[ Storage condition ]:
2-8°C

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
2811

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ HS Code ]:
2928000090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2928000090

[ Summary ]:
2928000090 other organic derivatives of hydrazine or of hydroxylamine VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

Articles

Fluorine-functionalized and simultaneously reduced graphene oxide as a novel hole transporting layer for highly efficient and stable organic photovoltaic cells.

Nanoscale 6(13) , 7183-7, (2014)

A one-step reduction and functionalization of graphene oxide (FrGO) was easily achieved using a novel phenylhydrazine-based reductant containing fluorine atoms, which can induce p-type doping due to i...

2-Substituted paullones: CDK1/cyclin B-inhibiting property and in vitro antiproliferative activity.

Bioorg. Med. Chem. Lett. 10(6) , 567-9, (2000)

9-Trifluoromethyl-paullones with a carbon chain in the 2-position were synthesized by palladium-catalyzed coupling reactions of a 2-iodoprecursor with terminal alkenes or alkynes, respectively. The in...


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Related Compounds

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