80938-67-6

Basic information

• Product Name: 5-PHENYL-O-TOLUIDINE
• Synonyms: 5-PHENYL-O-TOLUIDINE;2-methyl-5-phenylaniline
• CAS NO: 80938-67-6
• Molecular Formula: C₁₃H₁₃N
• Molecular Weight: 183.25
• Mol File: 80938-67-6.mol
• Article Data: 5

Chemical Properties

• Melting Point: 58 °C
• Boiling Point: 347.2 °C at 760 mmHg
• Flash Point: 177.7 °C
• Appearance: /
• Density: 1.057 g/cm³
• Vapor Pressure: 5.47E-05mmHg at 25°C
• Refractive Index: 1.607
• Storage Temp.: Sealed in dry,Room Temperature
• Sensitive: Air Sensitive
• CAS DataBase Reference: 5-PHENYL-O-TOLUIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-PHENYL-O-TOLUIDINE(80938-67-6)
• EPA Substance Registry System: 5-PHENYL-O-TOLUIDINE(80938-67-6)

Safety Data

• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 80938-67-6(Hazardous Substances Data)

Usage

General Description

5-Phenyl-O-toluidine is a chemical compound that is commonly used in the production of dyes, pharmaceuticals, and various other industrial applications. It is classified as a phenylamine, which is a type of organic compound that contains a phenyl group and an amino group. The chemical is known for its potential to cause skin and eye irritation, and its potential to be harmful if swallowed or inhaled. In addition, it has been identified as a potential carcinogen and mutagen. Due to these health risks, proper handling and protective equipment are necessary when working with 5-phenyl-O-toluidine.

InChI:InChI=1/C13H13N/c1-10-7-8-12(9-13(10)14)11-5-3-2-4-6-11/h2-9H,14H2,1H3

Upstream product

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Relevant articles and documents

Ligand-Free C–C Coupling Reactions Promoted by Hexagonal Boron Nitride-Supported Palladium(II) Catalyst in Water

A micron-scale palladium(II) material has been successfully prepared using Schiff base-modified hexagonal boron nitride as a support and used for the first time as an efficient and recyclable catalyst in organic synthesis. The morphology, composition, metal loading and thermal stability of the catalyst were studied using scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), infrared spectroscopy (FT-IR), inductively coupled plasma (ICP) and thermogravimetric (TG) analyses. Then, the micron material was tested in various C–C cross-coupling reactions and exhibited excellent catalytic activities in the Suzuki and Heck reactions. Moreover, the catalyst could be easily recovered by simple filtration and reused at least ten times without significant loss of its catalytic activity. In general, this work demonstrates the possibility of using Schiff-base@hexagonal boron nitride as an efficient support for heterogeneous catalysts. (Figure presented.).

NOVEL COMPOUND

A compound is represented by the following formula (1). In the formula (1), Ar is a substituted or unsubstituted aryl group including 6 to 30 ring carbon atoms, Ra are independently a substituted or unsubstituted alkyl group including 1 to 15 c

Palladium(II)-Schiff base complex immobilized covalently on h-BN: An efficient and recyclable catalyst for aqueous organic transformations

A moisture- and air-stable palladium(II)-Schiff base complex supported on h-BN was simply prepared by using commercially available reagents. This nanomaterial was applied as an excellent and recyclable heterogeneous catalyst for the Suzuki and Heck cross-coupling reactions. And it has been characterized by FT-IR, XRD, SEM, XPS, TG and ICP-AES techniques. High yields, ligand-free, low reaction time, water as solvent, non-toxicity and recyclability of the catalyst are the main merits of these protocols. In addition, a series of pharmacologically relevant products were successfully synthesized using this catalyst. Above all, this work opens up an interesting and attractive avenue for the use of h-BN as an efficient support for heterogeneous catalysts.