Search

  • Order Status
  • Quick Order
  • Promos
Element SearchElement SearchStructure SearchStructure Search
4,5,6,7-Tetrahydrobenzo[b]thiophene-2-carboxylic acid, 97%
4,5,6,7-Tetrahydrobenzo[b]thiophene-2-carboxylic acid, 97%
4,5,6,7-Tetrahydrobenzo[b]thiophene-2-carboxylic acid, 97%
Thermo Scientific Chemicals

4,5,6,7-Tetrahydrobenzo[b]thiophene-2-carboxylic acid, 97%

CAS: 40133-07-1 | C9H10O2S | 182.237 g/mol
Have Questions?
Change viewbuttonViewtableView
Quantity:
1 g
5 g
ChemDexTry the chem dexTM web app
Catalog number H33062.06
also known as H33062-06
Price (EUR)
284,00
Each
Quantity:
5 g
Request bulk or custom format
Price (EUR)
284,00
Each
Chemical Identifiers
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
View more
SpecificationsSpecification SheetSpecification Sheet
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.

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 .