41498-43-5

Basic information

• Product Name: phenanthrene-4-carbaldehyde
• Synonyms: phenanthrene-4-carbaldehyde;4-phenanthrenecarboxaldehyde
• CAS NO: 41498-43-5
• Molecular Formula: C15H10O
• Molecular Weight: 206.243
• Mol File: 41498-43-5.mol
• Article Data: 3

Chemical Properties

• Melting Point: 88-91 °C(Solv: ethyl ether (60-29-7))
• Boiling Point: 405.7°Cat760mmHg
• Flash Point: 269.2°C
• Appearance: /
• Density: 1.217g/cm³
• Vapor Pressure: 8.58E-07mmHg at 25°C
• Refractive Index: 1.745
• CAS DataBase Reference: phenanthrene-4-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: phenanthrene-4-carbaldehyde(41498-43-5)
• EPA Substance Registry System: phenanthrene-4-carbaldehyde(41498-43-5)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 41498-43-5(Hazardous Substances Data)

Usage

General Description

Phenanthrene-4-carbaldehyde is a chemical compound with the molecular formula C15H10O. It is a yellow crystalline solid with a distinctive aromatic odor. Phenanthrene-4-carbaldehyde is commonly used as a building block in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals. It is also used as a starting material for the synthesis of dyes and pigments. Additionally, it has been studied for its potential use in the fields of materials science and organic electronics. Phenanthrene-4-carbaldehyde is considered to be moderately toxic and should be handled with care in laboratory and industrial settings.

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 
• 832-64-4 4-methylphenanthrene 
• 71093-82-8 (Z)-m-Styryl-benzaldehyd 
• 178056-95-6 2-((E)-2-phenylethenyl)phenylboronic acid 
• 54737-45-0 (E)-2-bromostilbene 
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Relevant articles and documents

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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.

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