41498-43-5

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
Phenanthrene-4-carbaldehyde serves as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the development of new compounds with potential therapeutic and pesticidal properties, contributing to advancements in healthcare and agriculture.
Used in Dye and Pigment Industries:
As a starting material, phenanthrene-4-carbaldehyde is utilized in the production of dyes and pigments. Its aromatic nature and chemical reactivity make it suitable for creating a wide range of colorants used in different industries, including textiles, plastics, and printing inks.
Used in Materials Science and Organic Electronics:
Phenanthrene-4-carbaldehyde has been studied for its potential applications in materials science and organic electronics. Its properties are being explored for use in the development of new materials with specific electronic, optical, or structural characteristics, which could be applied in various high-tech devices and systems.

InChI:InChI=1/C15H10O/c16-10-13-6-3-5-12-9-8-11-4-1-2-7-14(11)15(12)13/h1-10H

Upstream product

• 22863-79-2 4‐phenanthrenemethanol 
• 178056-95-6 2-((E)-2-phenylethenyl)phenylboronic acid 
• 1080-32-6 O,O-diethyl benzylphosphonate 
• 54737-45-0 (E)-2-bromostilbene 
• 71093-82-8 (Z)-m-Styryl-benzaldehyd 
• 832-64-4 4-methylphenanthrene 

Relevant academic research and scientific papers

Polycyclic Aromatic Hydrocarbons via Iron(III)-Catalyzed Carbonyl-Olefin Metathesis

Polycyclic aromatic hydrocarbons are important structural motifs in organic chemistry, pharmaceutical chemistry, and materials science. The development of a new synthetic strategy toward these compounds is described based on the design principle of iron(III)-catalyzed carbonyl-olefin metathesis reactions. This approach is characterized by its operational simplicity, high functional group compatibility, and regioselectivity while relying on FeCl3 as an environmentally benign, earth-abundant metal catalyst. Experimental evidence for oxetanes as reactive intermediates in the catalytic carbonyl-olefin ring-closing metathesis has been obtained.

2-[(arylmethyl)amino]-2-methyl-1,3-propanediol DNA intercalators. An examination of the effects of aromatic ring variation on antitumor activity and DNA binding

The effects of variation of aromatic ring size, shape, and side-chain position on antitumor activity and DNA binding in a series of carbocyclic 2-[(arylmethyl)amino]-2-methyl-1,3-propanediols (AMAPs) were examined. In general, the interaction of AMAPs wit

Phenanthrene derivatives

The present invention relates to compounds of formula (1) or a monomethyl ether thereof (the compound of formula (1) including these ethers may contain no more than 30 carbon atoms in total); ethers, esters thereof; acid addition salts thereof; wherein Ar