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Thermo Scientific Chemicals
2,3,3,5-Tetramethylindolenine, 94%
CAS: 25981-82-2 | C12H15N | 173.26 g/mol
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Catalog number H33109.09
also known as H33109-09
Price (JPY)
-
Quantity:
10 g
Chemical Identifiers
CAS25981-82-2
IUPAC Name2,3,3,5-tetramethyl-3H-indole
Molecular FormulaC12H15N
InChI KeyRQVAPBRSUHSDGP-UHFFFAOYSA-N
SMILESCC1=NC2=CC=C(C)C=C2C1(C)C
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Specifications
Specification Sheet
Specification SheetRefractive Index1.5430-1.5510 @ 20°C
Appearance (Color)Clear orange to brown
Assay (GC)≥92.0%
FormLiquid
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.
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:
- 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 .
- 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 .