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Sku CI17344_1_G
Chem Impex
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Product Information

Product Name
1-Benzyl-1H-imidazole-5-carboxaldehyde
Brand Name
Chem Impex
Product Number
17344
CAS
85102-99-4
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
2773239
IUPAC Name
3-benzylimidazole-4-carbaldehyde
InChI Key
QONDAZCJAPQGRX-UHFFFAOYSA-N
SMILES
C1=CC=C(C=C1)CN2C=NC=C2C=O

Application

1-Benzyl-1H-imidazole-5-carboxaldehyde is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a key intermediate in synthesizing various pharmaceutical agents, particularly those targeting neurological disorders.

Organic Synthesis: It is commonly used in organic chemistry for the preparation of more complex molecules, allowing researchers to explore new chemical pathways.

Biochemical Research: The compound is valuable in studying enzyme interactions and metabolic pathways, providing insights into cellular processes.

Material Science: Its unique properties make it suitable for developing advanced materials, such as polymers and coatings, enhancing durability and functionality.

Analytical Chemistry: It is employed as a standard in various analytical techniques, aiding in the accurate quantification of related compounds in complex mixtures.

References Data Source From Pubchem

New synthesis of 3-amino-1H-benzo[f]chromene-2-carbonitriles

Publication Name: Russian Journal of Organic Chemistry
Publication Date: 2013-03
DOI: 10.1134/s1070428013030147

Synthesis, cytotoxicity and calcium antagonist activity of novel imidazolyl derivatives of 1,8-acridinediones

Publication Name: Journal of the Iranian Chemical Society
Publication Date: 2011-12
DOI: 10.1007/bf03246554

Synthesis and Ocular Effects of Imidazole Nitrolic Acids

Publication Name: Journal of Medicinal Chemistry
Publication Date: 2005-05-13
DOI: 10.1021/jm048949+

Cyclization of N-Monoacylated 1,2-Diaminoalkenes

Publication Name: Science of Synthesis
Publication Date: 2002