Ácido 4,5,6,7-tetrahidrobenzo[b]tiofeno-2-carboxílico, 97 %, Thermo Scientific Chemicals
Ácido 4,5,6,7-tetrahidrobenzo[b]tiofeno-2-carboxílico, 97 %, Thermo Scientific Chemicals
Ácido 4,5,6,7-tetrahidrobenzo[b]tiofeno-2-carboxílico, 97 %, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Ácido 4,5,6,7-tetrahidrobenzo[b]tiofeno-2-carboxílico, 97 %, Thermo Scientific Chemicals

CAS: 40133-07-1 | C9H10O2S | 182.237 g/mol
Have Questions?
Cambiar vistabuttonViewtableView
Cantidad:
1 g
5 g
Número de catálogo H33062.06
también denominado H33062-06
Precio (USD)
-
Cantidad:
5 g
Pedido a granel o personalizado
Identificadores químicos
CAS40133-07-1
IUPAC Name4,5,6,7-tetrahydro-1-benzothiophene-2-carboxylate
Molecular FormulaC9H9O2S
InChI KeyROLXOQXKNDKXTA-UHFFFAOYSA-M
SMILES[O-]C(=O)C1=CC2=C(CCCC2)S1
Ver más
EspecificacionesSpecification SheetHoja de especificaciones
Appearance (Color)White
Assay (Silylated GC)≥96.0%
Assay (Aqueous acid-base Titration)≥96.0 to ≤104.0%
FormCrystals or powder or crystalline powder
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 - Para uso exclusivo en investigación

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 .