95888-33-8

Basic information

• Product Name: Benzaldehyde, 2-(phenylamino)-
• CAS NO: 95888-33-8
• Molecular Formula: C13H11NO
• Molecular Weight: 197.236
• Mol File: 95888-33-8.mol
• Article Data: 19

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 2-(phenylamino)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 2-(phenylamino)-(95888-33-8)
• EPA Substance Registry System: Benzaldehyde, 2-(phenylamino)-(95888-33-8)

Safety Data

• Hazardous Substances Data: 95888-33-8(Hazardous Substances Data)

Upstream product

• 91-40-7 2-(phenylamino)benzoic acid 
• 591-50-4 iodobenzene 
• 529-23-7 o-aminobenzaldehyde 
• 6630-33-7 ortho-bromobenzaldehyde 
• 34824-58-3 2-(2-bromophenyl)-1,3-dioxolan 
• 62-53-3 aniline 
• 552-89-6 2-nitro-benzaldehyde 
• 271-58-9 anthranil 
• 98-80-6 phenylboronic acid 
• 29809-25-4 2-nitrosobenzaldehyde 
• 40138-16-7 2-formylbenzene boronic acid 
• 586-96-9 Nitrosobenzene 
• 590-28-3 potassium cyanate 
• 601520-18-7 3-butylamino-1,3-diphenyl-1H,3H-quinoline-2,4-dione 

Downstream Products

• 625-34-3 3-oxobutyraldehyde 
• 1246849-52-4 (E)-2-(phenylamino)benzaldehyde oxime 
• 206645-70-7 10-(4-methoxyphenyl) acridin-9(10H)-one 
• 578-95-0 10H-acridin-9-one 
• 1416427-14-9 2-((N-methyl-N-phenyl)amino)styrene 
• 208664-53-3 2-((N-methyl-N-phenyl)amino)benzaldehyde 
• 159661-93-5 (E)-4,5-dihydro-3-[[2-(phenylamino)phenyl]methylene]-2(3H)-furanone 
• 209412-70-4 [1-(2-Phenylamino-phenyl)-meth-(E)-ylideneaminooxy]-ethaneperoxoic acid tert-butyl ester 

Relevant articles and documents

Aza-aromatic polycycles based on triphenylene and acridine or acridone: Synthesis and properties

Acridine- and acridone-based polycyclic aromatics were prepared by using as the key steps a copper-catalysed N-arylation of 2-aminobenzaldehyde, 2-aminophenones, or ethyl 2-aminobenzoate with 2-iodotriphenylene, and an acid-mediated cyclization. The regioselectivity of this intramolecular SEAr reaction was studied by performing Hückel theory calculations on the precursors. Due to their structural similarity with some MALDI-MS matrices, two acridine-based polycycles were evaluated for this purpose. Finally, in view of structure-property relationships, preliminary studies of the photophysical properties of the synthesized acridine- and acridone-based polycycles were performed.

Access to acridones by tandem copper(i)-catalyzed electrophilic amination/Ag(i)-mediated oxidative annulation of anthranils with arylboronic acids

An efficient and practical approach for the synthesis of medicinally important acridones was developed from anthranils and commercially available arylboronic acids by a tandem copper(i)-catalyzed electrophilic amination/Ag(i)-mediated oxidative annulation strategy. This new and straightforward protocol displayed a broad substrate scope (25 examples) and high functional group tolerance. What's more, a possible mechanistic proposal was also presented.

Substituent Effect Induces Emission Modulation of Stilbene Photoswitches by Spatial Tuning of the N/B Electronic Constraints

We present a family of stilbene derivatives (1-4) ortho-functionalized with an electron donor and acceptor. Their emission was tuned by donor substitutions, dictating charge transfer dependent on the N···B spatial separation. The steric reduction of subst