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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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Catalog NumberQuantity
H33220.03
also known as H33220-03
1 g
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Catalog number H33220.03
also known as H33220-03
Price (USD)
162.00
Each
Quantity:
1 g
Request bulk or custom format
Price (USD)
162.00
Each
Chemical Identifiers
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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SpecificationsSpecification SheetSpecification Sheet
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.

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 .