3-Fluoro-5-(pentafluorothio)aniline, 97%, Thermo Scientific Chemicals
3-Fluoro-5-(pentafluorothio)aniline, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

3-Fluoro-5-(pentafluorothio)aniline, 97%, Thermo Scientific Chemicals

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Quantity:
250 mg
1 g
Catalog number H33680.MD
also known as H33680-MD
Price (USD)/ Each
188.00
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Quantity:
250 mg
Request bulk or custom format
Price (USD)/ Each
188.00
Add to cart
3-Fluoro-5-(pentafluorothio)aniline, 97%, Thermo Scientific Chemicals
Catalog numberH33680.MD
Price (USD)/ Each
188.00
-
Add to cart
Chemical Identifiers
CAS1240256-99-8
IUPAC Name3-fluoro-5-(pentafluoro-λ⁶-sulfanyl)aniline
Molecular FormulaC6H5F6NS
InChI KeyRFXWDLYDFAZNLO-UHFFFAOYSA-N
SMILESNC1=CC(F)=CC(=C1)S(F)(F)(F)(F)F
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SpecificationsSpecification SheetSpecification Sheet
FormCrystalline powder or fused solid
Melting Point (clear melt)34-40?C
Assay (GC)≥96.0%
Appearance (Color)White to pale cream or pale grey
It is used as pharmaceutical intermediate. Benzoylthiophenes are allosteric enhancers (AE) of agonist activity at the A1 adenosine receptor.

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
It is used as pharmaceutical intermediate. Benzoylthiophenes are allosteric enhancers (AE) of agonist activity at the A1 adenosine receptor.

Solubility
Sparingly soluble in water.(0.26 g/L) (25°C),

Notes
Store in cool dry place. Ensure proper ventilation. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. C. Elisabet Tranberg.; Andrea Zickgraf.; Brian N. Giunta.; Henning Luetjens.; Heidi Figler.; Lauren J. Murphree.; Ruediger Falke.; Holger Fleischer.; Joel Linden.; Peter J. Scammells.; Ray. A. Olsson. 2-Amino-3-aroyl-4,5-alkylthiophenes:  Agonist Allosteric Enhancers at Human A1 Adenosine Receptors.J. Med. Chem. 2002, 45 (2),382-389 .
  2. Robert H. Dodd.; Catherine Ouannes.; Malka Robert-Gero.; Pierre Potier. Hybrid molecules: growth inhibition of Leishmania donovani promastigotes by thiosemicarbazones of 3-carboxy-.beta.-carbolines.J. Med. Chem. 1989, 32 (6),1272-1276 .