3,5-Dichloro-1H-indazole, 95%, Thermo Scientific Chemicals
3,5-Dichloro-1H-indazole, 95%, Thermo Scientific Chemicals
3,5-Dichloro-1H-indazole, 95%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

3,5-Dichloro-1H-indazole, 95%, Thermo Scientific Chemicals

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Número de catálogoCantidad
H33220.03
también denominado H33220-03
1 g
Número de catálogo H33220.03
también denominado H33220-03
Precio (USD)
-
Cantidad:
1 g
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Identificadores químicos
CAS36760-20-0
IUPAC Name3,5-dichloro-2H-indazole
Molecular FormulaC7H4Cl2N2
InChI KeyQQZISIWJMCCCNH-UHFFFAOYSA-N
SMILESClC1=C2C=C(Cl)C=CC2=NN1
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EspecificacionesSpecification SheetHoja de especificaciones
Appearance (Color)White
FormPowder
Assay (HPLC)≥94.0%
Melting Point (clear melt)236.5-245.5?C
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.

Aplicaciones
Se utiliza como intermedio farmacéutico. Los benzoiltiofenos son potenciadores alostéricos (AE) de la actividad agonista en el receptor A1 de la adenosina.

Solubilidad
Poco soluble en agua.(0,26 g/l) (25 °C),

Notas
Almacenar en un lugar fresco y seco. Garantizar una ventilación adecuada. Incompatible con agentes oxidantes.
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 .