23645-37-6

Basic information

• Product Name: 1-Amino-2-phenylnaphthalene
• Synonyms: 1-Amino-2-phenylnaphthalene
• CAS NO: 23645-37-6
• Molecular Formula: C₁₆H₁₃N
• Molecular Weight: 219.28112
• Mol File: 23645-37-6.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 386.8°C at 760 mmHg
• Flash Point: 202.6°C
• Appearance: /
• Density: 1.147g/cm³
• Vapor Pressure: 3.46E-06mmHg at 25°C
• Refractive Index: 1.688
• CAS DataBase Reference: 1-Amino-2-phenylnaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Amino-2-phenylnaphthalene(23645-37-6)
• EPA Substance Registry System: 1-Amino-2-phenylnaphthalene(23645-37-6)

Safety Data

• Hazardous Substances Data: 23645-37-6(Hazardous Substances Data)

Usage

General Description

1-Amino-2-phenylnaphthalene, also known as α-aminonaphthalene or 2-naphthylamine, is a chemical compound with the molecular formula C16H13N. It is a pale yellow solid that is insoluble in water and commonly used in the production of dyes, pharmaceuticals, and agricultural products. 1-Amino-2-phenylnaphthalene is classified as a hazardous substance and is considered to be a potential carcinogen, with inhalation, ingestion, and skin contact presenting significant health risks. Exposure to this chemical has been linked to bladder and other types of cancer. Therefore, the use and handling of 1-Amino-2-phenylnaphthalene should be done with caution, maintaining proper protective measures to minimize the risk of harm to human health and the environment.

InChI:InChI=1/C16H13N/c17-16-14-9-5-4-8-13(14)10-11-15(16)12-6-2-1-3-7-12/h1-11H,17H2

Upstream product

• 771-14-2 2-bromonaphthalen-1-amine 
• 98-80-6 phenylboronic acid 
• 134-32-7 1-amino-naphthalene 
• 108-90-7 chlorobenzene 
• 2042-37-7 o-cyanobromobenzene 
• 86-57-7 1-Nitronaphthalene 
• 71-43-2 benzene 
• 74886-75-2 1-nitro-2-phenylnaphthalene 

Downstream Products

• 1152092-21-1 N-(2-bromo-3-methylphenyl)-2-phenylnaphthalen-1-amine 
• 1152092-15-3 N-(2-bromo-5-(trifluoromethyl)phenyl)-2-phenylnaphthalen-1-amine 
• 1152092-19-7 N-(2-bromo-5-chlorophenyl)-2-phenylnaphthalen-1-amine 
• 1152092-13-1 N-(2-bromo-5-methoxyphenyl)-2-phenylnaphthalen-1-amine 
• 1152092-17-5 N-(2-bromo-5-fluorophenyl)-2-phenylnaphthalen-1-amine 
• 1152092-11-9 N-(2-bromophenyl)-2-phenylnaphthalen-1-amine 

Relevant articles and documents

DIPROTONATION OF NITROARENES

Cryoscopic measurements shows that 1-nitronaphthalene is diprotonated in trifluoromethanesulfonic acid (TFSA).The diprotonated nitronaphthalenes are N,N-dihydroxyiminiumnaphthalenium dications, wich are fully characterised by UV, 1H-, 13/

Additive-free radical cascade reaction of oxime esters: Synthesis of pyrroline-functionalized phenanthridines

A variety of dihydropyrrole-functionalized phenanthridines were efficiently synthesized by the metal-free, radical cascade cyclization reaction of 2-isocyanobiphenyls with γ,δ- unsaturated oxime esters. The C-N/C-C/C-C bonds were formed via the oil bath method in a one-pot procedure with broad substrate applicability. The radical process was supported by kinetic isotope effect studies and radical inhibition studies.

Palladium-catalyzed asymmetric dearomatization of naphthalene derivatives

(Chemical Equation Presented) An intramolecular enantioselective metal-catalyzed dearomatization reaction is described. This procedure allows the dearomatization of naphthalene derivatives through an electrophilic aromatic substitution-type reaction on a