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Sku CI26147_100_MG
Chem Impex
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Product Information

Product Name
Thieno3,2-cpyridine
Brand Name
Chem Impex
Product Number
26147
CAS
272-14-0
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
67500
IUPAC Name
thieno3,2-cpyridine
InChI Key
MKYRMMMSZSVIGD-UHFFFAOYSA-N
SMILES
C1=CN=CC2=C1SC=C2

Description

Thieno3,2-cpyridine is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a key building block in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders and cancer.

Agricultural Chemistry: It is used in the formulation of agrochemicals, enhancing the efficacy of pesticides and herbicides, which helps in improving crop yields and protecting plants from pests.

Material Science: Thieno3,2-cpyridine is incorporated into organic electronic materials, contributing to the design of advanced devices such as organic solar cells and light-emitting diodes (LEDs).

Biochemical Research: Researchers utilize this compound to study various biological pathways, providing insights into enzyme interactions and cellular processes, which can lead to new therapeutic approaches.

Analytical Chemistry: It is employed as a reagent in analytical methods, aiding in the detection and quantification of other chemical substances, thus enhancing the accuracy of chemical analyses.

References Data Source From Pubchem

Cuproptosis: the mechanisms of copper-induced cell death and its implication in colorectal cancer

Publication Name: Naunyn-Schmiedeberg's Archives of Pharmacology
Publication Date: 2025-05-21
DOI: 10.1007/s00210-025-04263-z

Cuproptosis, ferroptosis and PANoptosis in tumor immune microenvironment remodeling and immunotherapy: culprits or new hope

Publication Name: Molecular Cancer
Publication Date: 2024-11-15
DOI: 10.1186/s12943-024-02130-8

Recent progress in photocatalytic NAD(P)H regeneration for photocatalytic-enzymatic-coupling system

Publication Name: Frontiers of Chemical Science and Engineering
Publication Date: 2024-03-19
DOI: 10.1007/s11705-024-2398-0

Synthesis of thieno[2,3-c]pyridine derived GRK2 inhibitors

Publication Name: Monatshefte für Chemie - Chemical Monthly
Publication Date: 2022-02-28
DOI: 10.1007/s00706-021-02889-2

Receptor-guided 3D-QSAR studies, molecular dynamics simulation and free energy calculations of Btk kinase inhibitors

Publication Name: BMC Systems Biology
Publication Date: 2017-03-14
DOI: 10.1186/s12918-017-0385-5