60709-95-7

Basic information

• Product Name: N-[4-(benzyloxy)phenyl]-N-phenylamine
• Synonyms: N-[4-(benzyloxy)phenyl]-N-phenylamine
• CAS NO: 60709-95-7
• Molecular Formula: C₁₉H₁₇NO
• Molecular Weight: 275.34438
• Mol File: 60709-95-7.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 443.7°Cat760mmHg
• Flash Point: 183.2°C
• Appearance: /
• Density: 1.146g/cm³
• Vapor Pressure: 4.55E-08mmHg at 25°C
• Refractive Index: 1.642
• CAS DataBase Reference: N-[4-(benzyloxy)phenyl]-N-phenylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-[4-(benzyloxy)phenyl]-N-phenylamine(60709-95-7)
• EPA Substance Registry System: N-[4-(benzyloxy)phenyl]-N-phenylamine(60709-95-7)

Safety Data

• Hazardous Substances Data: 60709-95-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C19H17NO/c1-3-7-16(8-4-1)15-21-19-13-11-18(12-14-19)20-17-9-5-2-6-10-17/h1-14,20H,15H2

Upstream product

• 100-44-7 benzyl chloride 
• 122-37-2 4-anilinophenol 
• 98-95-3 nitrobenzene 
• 146631-00-7 [4-(benzyloxy)phenyl]boronic acid 
• 100-39-0 benzyl bromide 

Downstream Products

• 60710-10-3 4-benzyloxy-N-benzyldiphenylamine 
• 60709-92-4 4'-benzyloxy-4-methoxy-N-phenylbenzanilide 
• 60709-99-1 4'-benzyloxy-N-phenylbenzanilide 
• 31310-73-3 N-phenyl-N-benzyl-p-aminophenol 
• 60710-15-8 Benzyl-[4-(2-dimethylamino-ethoxy)-phenyl]-phenyl-amine 
• 60710-21-6 4-benzyloxy-N-(4-methoxybenzyl)diphenylamine 
• 60710-23-8 4-(2-Diethylaminoethoxy)-N-(4-methoxybenzyl)diphenylamine 
• 60709-94-6 N-[4-(3-Dimethylamino-propoxy)-phenyl]-4-methoxy-N-phenyl-benzamide 
• 60709-98-0 4'-(3-dimethylaminopropoxy)-4-chloro-N-phenylbenzanilide 
• 60710-11-4 Benzyl-[4-(2-diethylamino-ethoxy)-phenyl]-phenyl-amine 
• 60710-18-1 Benzyl-[4-(3-dimethylamino-propoxy)-phenyl]-phenyl-amine 
• 60709-93-5 N-(4-Hydroxy-phenyl)-4-methoxy-N-phenyl-benzamide 
• 60709-97-9 4'-hydroxy-4-chloro-N-phenylbenzanilide 
• 60710-22-7 4-hydroxy-N-(4-methoxybenzyl)diphenylamine 

Relevant articles and documents

PEt3-mediated deoxygenative C–N coupling of nitroarenes and boronic acids

A method for the preparation of aryl- and heteroarylamine products by triethylphosphine-mediated deoxygenative coupling of nitroarenes and boronic acids is reported. This method provides access to an array of functionalized (hetero)arylamine products from readily available starting materials under the action of an inexpensive commercial reagent. The developed triethylphosphine-mediated transformation highlights the capability of organophosphorus compounds to carry out this useful deoxygenative transformation without the necessity of any transition metal additives.

New indolizine compound, preparation method thereof and pharmaceutical compositions containing them (by machine translation)

The invention of the formula (I) compound, Wherein R a, R b, R c, R d, T, R 3, R 4, R 5, X, Y and Het as defined in the description. The invention also relates to a medicament containing the above-mentioned compounds. (by machine translation)

INDOLIZINE COMPOUNDS, A PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

Compounds of formula (I) wherein Ra, Rb, Rc, Rd, T, R3, R4, R5, X, Y and Het are as defined in the description. Medicinal products containing the same which are useful in treating pathologies involving a deficit in apoptosis, such as cancer, auto-immune diseases, and diseases of the immune system.