24007-66-7

Basic information

• Product Name: N-(p-Aminobenzyl)aniline
• Synonyms: N-(p-Aminobenzyl)aniline
• CAS NO: 24007-66-7
• Molecular Formula: C₁₃H₁₄N₂
• Molecular Weight: 198.2637
• Mol File: 24007-66-7.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 373°Cat760mmHg
• Flash Point: 211.4°C
• Appearance: /
• Density: 1.153g/cm³
• Vapor Pressure: 9.22E-06mmHg at 25°C
• Refractive Index: 1.675
• CAS DataBase Reference: N-(p-Aminobenzyl)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-(p-Aminobenzyl)aniline(24007-66-7)
• EPA Substance Registry System: N-(p-Aminobenzyl)aniline(24007-66-7)

Safety Data

• Hazardous Substances Data: 24007-66-7(Hazardous Substances Data)

Usage

General Description

N-(p-Aminobenzyl)aniline is a chemical compound with the molecular formula C13H14N2. It is a crystalline solid with a faint odor, and it is commonly used as an intermediate in the synthesis of various pharmaceuticals and dyes. N-(p-Aminobenzyl)aniline is also known for its ability to act as a colorimetric reagent for the determination of certain transition metals, such as cadmium and zinc. N-(p-Aminobenzyl)aniline is considered to be hazardous if ingested or inhaled and can cause irritation to the respiratory system, skin, and eyes. As such, proper handling and safety precautions should be taken when working with this chemical.

InChI:InChI=1/C13H14N2/c14-12-8-6-11(7-9-12)10-15-13-4-2-1-3-5-13/h1-9,15H,10,14H2

Upstream product

• 142-04-1 aniline hydrochloride 
• 91-78-1 1,3,5-triphenylhexahydro-1,3,5-triazine 
• 62-53-3 aniline 
• 71840-36-3 chloromethylmercurioacetaldehyde 
• 239074-27-2 4-(1,1-dimethylethoxycarbonylamino)benzylbromide 
• 622-14-0 N,N'-diphenylmethylenediamine 
• 555-16-8 4-nitrobenzaldehdye 
• 3460-11-5 4-nitrobenzanilide 
• 782-45-6 4-amino-benzoic acid anilide 
• 785-80-8 p-nitrobenzylideneaniline 
• 10359-18-9 N-(4-nitrobenzyl)aniline 
• 64-19-7 acetic acid 
• 88933-19-1 methoxymethylphenylamine 
• 63516-03-0 α-bromo-p-toluidine 

Downstream Products

• 22005-18-1 4-(4-amino-benzyl)-6-methyl-m-phenylenediamine 
• 64497-21-8 2-methylbis-(4-aminophenyl)methane 
• 101-77-9 4,4'-diamino diphenyl methane 
• 83322-98-9 (4-amino-phenyl)-(4-dimethylamino-phenyl)-methane 
• 83215-18-3 4-aniline 
• 83215-16-1 4-(4-anilinomethylanilinomethyl)aniline 
• 83215-17-2 α-hydro-ω-anilinotris(imino-1,4-phenylenemethylene) 
• 62-53-3 aniline 
• 6278-73-5 2-(4-aminophenyl)benzothiazole 

Relevant articles and documents

Polymer-supported palladium-imidazole complex catalyst for hydrogenation of substituted benzylideneanilines

The polymer-supported palladium-imidazole complex catalyst was synthesized and characterized by various techniques such as elemental analysis, IR spectroscopy and TG analysis. The physico-chemical properties such as bulk density, surface studies by BET me

Lewis acid solid catalysts for the synthesis of methylenedianiline from aniline and formaldehyde

A catalyst containing Hf4+ and Zn2+ supported on silica has been found to be highly effective for the synthesis of methylenedianiline (MDA), an indispensable precursor in the polyurethane industry. Its performance was further improved when the silica support was replaced by silica-alumina, which resulted in a catalyst that was both active and selective, as indicated by the high MDA yield and high 4,4′–MDA/(2,2′–MDA + 2,4′–MDA) isomer ratio obtained. Furthermore, the catalyst also gave an appreciable oligomeric MDA (OMDA) yield and was noticeably more stable than the zeolites that were used in comparative tests: it could be used in at least five consecutive runs without any significant loss in activity. The combination of Br?nsted and Lewis acidity strongly increases the overall activity and yields a catalyst that represents a remarkably stable and reusable alternative to the commonly studied systems for this reaction.

N-(4-substituted phenyl)-2-substituted acetamide compound and is use as SIRT2 protein inhibitor

The invention discloses a compound shown in the formula I or its pharmaceutically acceptable salt, crystalline form and solvate. X represents a group shown in the description, Y represents a group shown in the description, R1, R2 and R3 independently represent H, hydroxyl, halogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkyl or phenyl, and R4 represents aryl, heteroaryl, substituted aryl or substituted heteroaryl. The novel compound shown in the formula I has good inhibition activity to SIRT2 and tumors, has a good medicinal value and provides a novel potential choice for clinical medication.