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Sku CI28274_25_G
Chem Impex
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Product Information

Product Name
5-Bromoquinoline
Brand Name
Chem Impex
Product Number
28274
CAS
4964-71-0
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
817321
IUPAC Name
5-bromoquinoline
InChI Key
CHODTZCXWXCALP-UHFFFAOYSA-N
SMILES
C1=CC2=C(C=CC=N2)C(=C1)Br

Application

5-Bromoquinoline is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-malarial and anti-cancer drugs, enhancing therapeutic efficacy.

Material Science: It is used in the creation of specialized materials, including organic semiconductors and light-emitting diodes (LEDs), due to its unique electronic properties.

Analytical Chemistry: 5-Bromoquinoline acts as a fluorescent probe in analytical techniques, aiding in the detection of metal ions and other analytes, which is crucial for environmental monitoring.

Biological Research: The compound is employed in studies investigating enzyme inhibition and receptor binding, providing insights into biological pathways and potential therapeutic targets.

Organic Synthesis: It is a valuable building block in organic synthesis, allowing chemists to create complex molecules efficiently, which can lead to innovations in various chemical products.

References Data Source From Pubchem

Quinoline: A Novel Solution for Next-Generation Pesticides, Herbicides, and Fertilizers

Publication Name: Applied Biochemistry and Biotechnology
Publication Date: 2025-01-04
DOI: 10.1007/s12010-024-05164-2

Synthetic account on indoles and their analogues as potential anti-plasmodial agents

Publication Name: Molecular Diversity
Publication Date: 2024-05-06
DOI: 10.1007/s11030-024-10842-8

Copper catalysis in the synthesis of N-naphthyl and N-quinolinyl derivatives of adamantane-containing amines

Publication Name: Russian Chemical Bulletin
Publication Date: 2023-11
DOI: 10.1007/s11172-023-4065-x

Ortho-C–H methoxylation of aryl halides enabled by a polarity-reversed N–O reagent

Publication Name: Nature Chemistry
Publication Date: 2023-08-31
DOI: 10.1038/s41557-023-01312-z