2-(Trifluoromethyl)phenylhydrazine, 97%
2-(Trifluoromethyl)phenylhydrazine, 97%
2-(Trifluoromethyl)phenylhydrazine, 97%
Thermo Scientific Chemicals

2-(Trifluoromethyl)phenylhydrazine, 97%

CAS: 365-34-4 | C7H7F3N2 | 176.142 g/mol
Have Questions?
Change viewbuttonViewtableView
Quantity:
1 g
5 g
Catalog number A14781.06
also known as A14781-06
Price (EUR)
113,00
Each
Quantity:
5 g
Request bulk or custom format
Price (EUR)
113,00
Each
Chemical Identifiers
CAS365-34-4
IUPAC Name1-phenyl-2-(trifluoromethyl)hydrazine
Molecular FormulaC7H7F3N2
InChI KeyLJORWWOXCXNLOT-UHFFFAOYSA-N
SMILESFC(F)(F)NNC1=CC=CC=C1
View more
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to yellow or cream to brown
FormCrystals or powder or crystalline powder
Assay (GC)≥96.0%
Melting Point (clear melt)58.0-67.0°C
2-(Trifluoromethyl)phenylhydrazine is used as an intermediate in organic syntheses. It is also ued as a fine chemical intermediate, GC derivatizing agent, coupling reagent and N- protecting agent.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
2-(Trifluoromethyl)phenylhydrazine is used as an intermediate in organic syntheses. It is also ued as a fine chemical intermediate, GC derivatizing agent, coupling reagent and N- protecting agent.

Solubility
Insoluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from strong oxidizing agents.
RUO – Research Use Only

General References:

  1. C Kunick.; C Schultz.; T Lemcke.; DW Zaharevitz. 2-Substituted paullones: CDK1/cyclin B-inhibiting property and in vitro antiproliferative activity. Bioorganic & Medicinal Chemistry Letters. 1999, 10 (6), 567-569.
  2. H Jiang.; Y Wang.; W Wan.; J Hao. p-TsOH promoted Fischer indole synthesis of multi-substituted 2-trifluoromethyl indole derivatives. Tetrahedron. 2010, 10 (6), 567-569.