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412295

Sigma-Aldrich

4-(Trifluoromethyl)phenylhydrazine

96%

Synonym(s):

1-(4-Trifluoromethylphenyl)hydrazine, 4-Trifluoromethylphenylhydrazine, [4-(Trifluoromethyl)phenyl]hydrazine, p-Trifluoromethylphenylhydrazine

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About This Item

Linear Formula:
CF3C6H4NHNH2
CAS Number:
368-90-1
Molecular Weight:
176.14
MDL number:
MFCD00042508
UNSPSC Code:
12352100
PubChem Substance ID:
24865801
NACRES:
NA.22

Quality Level

200

Assay

96%

bp

118-122 °C/17 mmHg (lit.)

mp

63-65 °C (lit.)

storage temp.

2-8°C

SMILES string

NNc1ccc(cc1)C(F)(F)F

InChI

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

InChI key

DBNLGTYGKCMLLR-UHFFFAOYSA-N

General description

4-(Trifluoromethyl)phenylhydrazine participates as phenylhydrazine-based reductant containing fluorine atoms in the one-step reduction and functionalization of graphene oxide.

Application

4-(Trifluoromethyl)phenylhydrazine may be used for the synthesis of 2-iodo-9-trifluoromethyl-paullone.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Su-Hyeon Kim et al.
Nanoscale, 6(13), 7183-7187 (2014-05-08)
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 its high electronegativity. The FrGO-based OPV exhibited a high power conversion efficiency of
C Kunick et al.
Bioorganic & medicinal chemistry letters, 10(6), 567-569 (2000-03-31)
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 introduction of a 2-cyanoethyl substituent led to a significant enhancement of CDK1/cyclin B inhibiting property and

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