127404-22-2

Basic information

• Product Name: [1,1',3',1",3",1"'-Quaterphenyl]-3,3'''-dicarbonaldehyde
• Synonyms: 3-(5-Methoxy-1H-indol-1-yl)benzaldehyde;3-(5-Nitro-1H-indol-1-yl)benzaldehyde;3-(6-(Methoxycarbonyl)-1H-indol-1-yl)benzaldehyde;3-(6-Chloro-1H-indol-1-yl)benzaldehyde;3-(6-Cyano-1H-indol-1-yl)benzaldehyde;3-(6-Fluoro-1H-indol-1-yl)benzaldehyde;3-(6-Methoxy-1H-indol-1-yl)benzaldehyde;3-(6-Nitro-1H-indol-1-yl)benzaldehyde
• CAS NO: 127404-22-2
• Molecular Formula: C₁₀H₈N₂O
• Molecular Weight: 172.19
• Mol File: 127404-22-2.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 356.9 °C at 760 mmHg
• Flash Point: 169.7 °C
• Appearance: Light yellow powder
• Density: 1.15g/cm³
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 5.26±0.10(Predicted)
• CAS DataBase Reference: [1,1',3',1",3",1"'-Quaterphenyl]-3,3'''-dicarbonaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: [1,1',3',1",3",1"'-Quaterphenyl]-3,3'''-dicarbonaldehyde(127404-22-2)
• EPA Substance Registry System: [1,1',3',1",3",1"'-Quaterphenyl]-3,3'''-dicarbonaldehyde(127404-22-2)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 127404-22-2(Hazardous Substances Data)

Usage

General Description

[1,1',3',1",3",1"'-Quaterphenyl]-3,3'''-dicarbonaldehyde is a chemical compound with the molecular formula C52H34O2. It is a dicarbonaldehyde derivative of quaterphenyl, which is a polycyclic aromatic hydrocarbon. [1,1',3',1",3",1"'-Quaterphenyl]-3,3'''-dicarbonaldehyde is used in organic synthesis and material science as a building block for the synthesis of various organic compounds and polymers. It has potential applications in the development of advanced materials such as liquid crystals, organic semiconductors, and optoelectronic devices. Additionally, it may also be used as a fluorescent probe for studies in biochemistry and cell biology. However, its specific properties and applications may vary depending on its purity, concentration, and the specific chemical and physical conditions in which it is used.

Upstream product

• 288-32-4 1H-imidazole 
• 696-41-3 m-iodobenzaldehyde 
• 3132-99-8 m-bromobenzoic aldehyde 
• 17789-14-9 3-(1,3-dioxolan-2-yl)-phenylbromide 
• 151055-85-5 2-<3-(1H-imidazol-1-yl)phenyl>-1,3-dioxolane 

Downstream Products

• 1396789-57-3 C₂₈H₃₁ClN₄OS 
• 131230-89-2 1,4-dihydro-2,6-dimethyl-4-<3-(1H-imidazol-1-yl)phenyl>-3,5-pyridinecarboxylic acid diethyl ester 
• 185908-04-7 4-(3-1H-imidazol-1-yl-phenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarbonitrile 
• 148612-77-5 1,4-dihydro-2-<(2-phthalimidoethoxy)methyl>-6-methyl-4-<3-(1H-imidazol-1-yl)phenyl>-3,5-pyridinedicarboxylic acid 3-ethyl 5-methyl ester 

Relevant articles and documents

Ultrafast singlet - singlet energy transfer in self-assembled via metal - ligand axial coordination of free-base porphyrin - zinc phthalocyanine and free-base porphyrin - zinc naphthalocyanine Dyads

Singlet - singlet energy transfer in self-assembled via axial coordination of imidazole-appended (at different positions of one of the meso-phenyl entities) free-base tetraphenylporphyrin, H2PIm, to either zinc phthalocyanine, ZnPc, or zinc nap

Magnetically retrievable lepidocrocite supported copper oxide nanocatalyst (Fe-CuO) for N-arylation of imidazole

A simple and efficient lepidocrocite-supported copper oxide catalyst (Fe-CuO) has been successfully prepared by a simple precipitation method in aqueous medium from readily available inexpensive starting materials and was used as a heterogeneous nanocatal

Imidazol-1-yl and Pyridin-3-yl Derivatives of 4-Phenyl-1,4-dihydropyridines Combining Ca2+ Antagonism and Thromboxane A2 Synthase Inhibition

A series of derivatives of 4-phenyl-1,4-dihydropyridine bearing imidazol-1-yl or pyridin-3-yl moieties on the phenyl ring were synthesized with the aim of combining Ca2+ antagonism and thromboxane A2 (Tx A2) synthase inhib