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Sku CI19838_1_G
Chem Impex
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Product Information

Product Name
1H-Pyrazolo3,4-cpyridine
Brand Name
Chem Impex
Product Number
19838
CAS
271-47-6
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
6451441
IUPAC Name
1H-pyrazolo5,4-cpyridine
InChI Key
KNYHISBJRQVMAZ-UHFFFAOYSA-N
SMILES
C1=CN=CC2=C1C=NN2

Description

1H-Pyrazolo3,4-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 anti-inflammatory and anti-cancer agents.

Agricultural Chemistry: It is used in the formulation of agrochemicals, contributing to the design of effective pesticides and herbicides that enhance crop protection.

Material Science: The compound is explored for its potential in creating novel materials, including polymers with unique properties for use in coatings and adhesives.

Biochemical Research: Researchers utilize it to study enzyme inhibition and receptor interactions, aiding in the understanding of biological processes and disease mechanisms.

Diagnostic Applications: It is being investigated for its role in developing diagnostic tools, particularly in the detection of certain diseases through innovative biochemical assays.

References Data Source From Pubchem

Recent progress on the excited-state multiple proton transfer process in organic molecules

Publication Name: Science China Chemistry
Publication Date: 2022-08-29
DOI: 10.1007/s11426-022-1375-y

Psychotropic Effects of a New Pyrazolo[C]Pyridine Derivate GIZh-72 are Related to Functional Activity of Atp-Sensitive Potassium Channels

Publication Name: Bulletin of Experimental Biology and Medicine
Publication Date: 2020-02
DOI: 10.1007/s10517-020-04729-5

Synthesis of fused pyrazoles via intramolecular cyclization of appropriately ortho-substituted nitroarenes and nitroheteroarenes

Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2017-02
DOI: 10.1007/s10593-017-2028-6

Synthesis of the Novel Tetrahydropyrazolo[3,4-c]pyridin-5-one Scaffold

Publication Name: Synlett
Publication Date: 2014-12-02
DOI: 10.1055/s-0034-1379504

Quantitative structure–activity relationship and design of polysubstituted quinoline derivatives as inhibitors of phosphodiesterase 4

Publication Name: Medicinal Chemistry Research
Publication Date: 2011-11-11
DOI: 10.1007/s00044-011-9831-x