CAS 27685-92-3
:thieno[3,2-c]pyridin-4(5H)-one
Description:
Thieno[3,2-c]pyridin-4(5H)-one is a heterocyclic organic compound characterized by a fused ring system that includes both a thiophene and a pyridine moiety. This compound features a carbonyl group at the 4-position of the pyridine ring, contributing to its reactivity and potential biological activity. It is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. The presence of the sulfur atom in the thiophene ring can influence its electronic properties, making it of interest in various fields, including medicinal chemistry and materials science. Thieno[3,2-c]pyridin-4(5H)-one derivatives have been studied for their potential pharmacological activities, including anti-inflammatory and anti-cancer properties. The compound's structure allows for various substitutions, which can further modify its chemical behavior and biological activity. As with many heterocycles, it may also participate in various chemical reactions, such as electrophilic aromatic substitution or nucleophilic addition, depending on the functional groups present.
Formula:C7H5NOS
InChI:InChI=1/C7H5NOS/c9-7-5-2-4-10-6(5)1-3-8-7/h1-4H,(H,8,9)
SMILES:c1cnc(c2ccsc12)O
Synonyms:- Thieno[3,2-c]pyridin-4-ol
- 5H-thieno[3,2-c]pyridin-4-one
- Thieno[3,2-c]pyridin-4(5H)-one
- 4-OXO-4,5-DIHYDROTHIENO[3,2-C]PYRIDINE
- 4-HYDROXYTHIENO[3,2-C]PYRIDINE
- 4,5-Dihydrothieno[3,2-c]pyridine-4-one
- 4H,5H-thieno[3,2-c]pyridin-4-one
- 1. 4-Hydroxythieno[3,2-c]pyridine
- 4-HYDROXYTHIENO[3,2-C]PYRIDINE ISO 9001:2015 REACH
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.
THIENO[3,2-C]PYRIDIN-4(5H)-ONE
CAS:Formula:C7H5NOSPurity:97%Color and Shape:SolidMolecular weight:151.18574-Hydroxythieno[3,2-c]pyridine
CAS:Formula:C7H5NOSPurity:97%Color and Shape:SolidMolecular weight:151.18Thieno[3,2-c]pyridin-4-ol
CAS:<p>Thieno[3,2-c]pyridin-4-ol is a thienopyridone that is an inhibitor of the bromodomain. It has been shown to inhibit the bromodomain, which is a protein domain that also binds acetylated histones. The inhibition of this domain leads to chromatin condensation and DNA compaction, inhibiting transcription and replication. Thieno[3,2-c]pyridin-4-ol has been shown to have anti-inflammatory effects in vivo and in vitro.</p>Formula:C7H5NOSPurity:Min. 95%Molecular weight:151.19 g/mol



