138253-30-2

Basic information

• Product Name: 4-(2,2':6',2''-TERPYRIDIN-4'-YL)BENZALDEHYDE
• Synonyms: 4-(2,2':6',2''-TERPYRIDIN-4'-YL)BENZALDEHYDE;4-(2, 2':6', 2"-Terpyridin-4'-yl)benzaldehyde 97%;4'-(4-formylphenyl)-[2,2':6',2'']-terpyridine;4-(2,6-di(pyridin-2-yl)pyridin-4-yl)benzaldehyde;4-(2,2':6',2''-terpyridine-4'-yl)benzaldehyde
• CAS NO: 138253-30-2
• Molecular Formula: C₂₂H₁₅N₃O
• Molecular Weight: 337.37
• Mol File: 138253-30-2.mol
• Article Data: 17

Chemical Properties

• Boiling Point: 525.9 °C at 760 mmHg
• Flash Point: 265.9 °C
• Appearance: /
• Density: 1.219 g/cm³
• PKA: 4.48±0.22(Predicted)
• CAS DataBase Reference: 4-(2,2':6',2''-TERPYRIDIN-4'-YL)BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2,2':6',2''-TERPYRIDIN-4'-YL)BENZALDEHYDE(138253-30-2)
• EPA Substance Registry System: 4-(2,2':6',2''-TERPYRIDIN-4'-YL)BENZALDEHYDE(138253-30-2)

Safety Data

• Hazardous Substances Data: 138253-30-2(Hazardous Substances Data)

Usage

General Description

4-(2,2':6',2''-terpyridin-4'-yl)benzaldehyde is a chemical compound with the molecular formula C28H20N4O. It is a member of the terpyridine family, which is a class of nitrogen-containing heterocycles. This particular compound contains a benzaldehyde group attached to a terpyridine backbone. Terpyridine compounds are known for their strong coordinating ability with metal ions, and their use in applications such as catalysis, molecular recognition, and supramolecular chemistry. The presence of the benzaldehyde group in 4-(2,2':6',2''-terpyridin-4'-yl)benzaldehyde suggests that it may have potential applications in organic synthesis and as a building block for the construction of more complex molecules.

Upstream product

• 89972-78-1 4'-(4-bromomethylphenyl)-2,2':6',2''-terpyridine 
• 87199-17-5 4-formylphenylboronic acid, 
• 134653-69-3 4'-{[(Trifluoromethyl)sulfonyl]oxy}-2,2':6',2''-terpyridine 
• 89972-77-0 4'-(4-methylphenyl)-2,2':6',2-terpyridine 
• 1122-62-9 2-acetylpyridine 
• 100-52-7 benzaldehyde 
• 104-87-0 4-methyl-benzaldehyde 
• 1228765-22-7 4'-(4-(dibromomethyl)phenyl)-2,2':6',2''-terpyridine 
• 623-27-8 terephthalaldehyde, 
• 52010-97-6 4-(hydroxylmethyl)benzaldehyde 
• 447399-94-2 4′-(4-hydroxymethylphenyl)-2,2′:6′,2′′-terpyridine 
• 81172-89-6 terephthalaldehyde mono(diethylacetal) 

Downstream Products

• 138253-31-3 5,15-Bis(3,5-di-tert-butylphenyl)-2,8,12,18-tetraethyl-3,7,13,17-tetramethylporphyrin 
• 138253-32-4 (1Z,4Z,9Z,15Z)-5-(3,5-Di-tert-butyl-phenyl)-2,8,12,18-tetraethyl-3,7,13,17-tetramethyl-15-(4-[2,2';6',2'']terpyridin-4'-yl-phenyl)-porphyrin 
• 138253-33-5 5,15-bis<4-(4'-phenyl-2,2':6',2''-terpyridinyl)>-3,7,13,17-tetraethyl-2,8,12,18-tetramethylporphyrin 
• 1353027-30-1 ((NO₂)2C₆H₃NHNCHC₆H₄)C₁₅H₁₀N₃ 
• 871118-49-9 4'-[4-(4,5-diphenyl-1H-imidazol-2-yl)-phenyl]-[2,2':6',2'']terpyridine 
• 1350456-12-0 2-(4-[2,2':6',2'']terpyridine-4'-yl-phenyl)-1H-phenanthro[9,10-d]-imidazole 
• 1350933-95-7 C₄₀H₃₉N₅O₄ 
• 1350933-97-9 C₃₆H₃₁N₅O₂ 
• 1350933-96-8 C₃₆H₃₁N₅O₄ 
• 1610833-64-1 (E)-3-(3-(4-([2,2′:6′,2″-terpyridin]-4′-yl)phenyl)acryloyl)-7-(diethylamino)-2H-chromen-2-one 
• 1621252-51-4 (5Z)-3-methyl-2-methylthio-5-[4-(2,2':6',2''-terpyridin-4'-yl)benzylidene]-3,5-dihydro-4H-imidazol-4-one 
• 1621252-49-0 (5Z)-3-methyl-5-[4-(2,2':6',2''-terpyridin-4'-yl)benzylidene]-2-thioxoimidazolidin-4-one 
• 1621252-52-5 (5Z)-2-methylthio-3-phenyl-5-[4-(2,2':6',2''-terpyridin-4'-yl)benzylidene]-3,5-dihydro-4H-imidazol-4-one 
• 1621252-50-3 (5Z)-3-phenyl-5-[4-(2,2':6',2''-terpyridin-4'-yl)benzylidene]-2-thioxoimidazolidin-4-one 

Relevant articles and documents

Transition-Metal Chelates of Terpyridine-Fullerene/Nanotube Diads: Synthesis and Redox Properties

The authors discuss the synthesis of two carbon cluster-based chelating tridentate ligands, terpyridyl-pyrrolidine-fullerene (C60-tpy) and terpyridyl-pyrrolidine multiwalled carbon nanotube (MWCNT-tpy), by 1,3-dipolar cycloaddition. The two che

One pot synthesis of formyl phenyl terpyridine: A simplified synthesis

Formyl phenylterpyridinewas synthesized from methyl phenylterpyridine using SeO2 as the oxidizing agent. SeO2 conventionally has been used to oxidize allylic and aliphatic methyl groups. The simple conversion of methyl group attached

A ternary memory module using low-voltage control over optical properties of metal-polypyridyl monolayers

A ternary memory module has been designed as a function of precise voltage command. The monolayer based module displays perpetual stability and non-hysteretic reversibility for multiple scans (102). Ternary-state readout provides a vision to integrate the next generation of "smart electro-optical devices" viable for multi-state memory. This journal is the Partner Organisations 2014.

Rigid π-Conjugated mono-, bis-, and tris(2,2′:6′,2″- terpyridines)

A set of rigid, π-conjugated linear mono- and bisterpyridines and star-shaped tristerpyridines have been synthesized using Pd(0)-catalyzed coupling reactions and the Horner -Wadsworth-Emmons reaction. The terpyridyl ligands obtained feature strong emissio

Preparation method and application of polypyridyl functional group modified porphyrin TTPP

The invention relates to the technical field of synthesis and application of polypyridyl porphyrins, and provides a preparation method and an application of a polypyridyl functional group modified porphyrin TTPP. The preparation method comprises the follo