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Sku CI21543_100_G
Chem Impex
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Product Information

Product Name
5-Benzyloxyindole-3-carboxaldehyde
Brand Name
Chem Impex
Product Number
21543
CAS
6953-22-6
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
81398
IUPAC Name
5-phenylmethoxy-1H-indole-3-carbaldehyde
InChI Key
DJGNUBADRQIDNQ-UHFFFAOYSA-N
SMILES
C1=CC=C(C=C1)COC2=CC3=C(C=C2)NC=C3C=O

Description

5-Benzyloxyindole-3-carboxaldehyde is widely utilized in research focused on:

Synthesis of Indole Derivatives: This compound serves as a key intermediate in the synthesis of various indole derivatives, which are important in pharmaceuticals and agrochemicals.

Pharmaceutical Research: It is explored for its potential therapeutic effects, particularly in developing new drugs targeting cancer and neurological disorders.

Fluorescent Probes: The compound can be modified to create fluorescent probes used in biological imaging, helping researchers visualize cellular processes.

Material Science: In the development of organic light-emitting diodes (OLEDs), this chemical can be incorporated into materials that enhance light emission efficiency.

Biochemical Studies: It is used in studies examining enzyme interactions and metabolic pathways, providing insights into biological functions and disease mechanisms.

References Data Source From Pubchem

Multimodal action of KRP203 on phosphoinositide kinases in vitro and in cells

Publication Name: Biochemical and Biophysical Research Communications
Publication Date: 2023-10-30
DOI: 10.1016/j.bbrc.2023.08.050

A quantitative high-throughput screen identifies compounds that lower expression of the SCA2-and ALS-associated gene ATXN2

Publication Name: The Journal of biological chemistry
Publication Date: 2022-08
DOI: 10.1016/j.jbc.2022.102228

Synthesis from Alkynes and 3-Formyl- or 3-Acetyl-1H-indoles

Publication Name: Science of Synthesis
Publication Date: 2021

New indole and indazole derivatives as potential antimycobacterial agents

Publication Name: Medicinal Chemistry Research
Publication Date: 2019-02-08
DOI: 10.1007/s00044-019-02293-w

C4 Pictet–Spengler Reactions for the Synthesis of Core Structures in Hyrtiazepine Alkaloids

Publication Name: Synthesis
Publication Date: 2017-06-07
DOI: 10.1055/s-0036-1588438