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

A Modular Flow Design for the meta-Selective C?H Arylation of Anilines

Described herein is an effective and practical modular flow design for the meta-selective C?H arylation of anilines. The design consists of four continuous-flow modules (i.e., diaryliodonium salt synthesis, meta-selective C?H arylation, inline copper extraction, and aniline deprotection) which can be operated either individually or consecutively to provide direct access to meta-arylated anilines. With a total residence time of 1 hour, the desired product could be obtained in high yield and excellent purity without the need for column chromatography, and the residual copper content meets the standards for parenterally administered pharmaceutical substances.

Novel cyclodextrin-modified h-BN@Pd(II) nanomaterial: An efficient and recoverable catalyst for ligand-free C-C cross-coupling reactions in water

An environmentally friendly palladium(II) catalyst supported on cyclodextrin-modified h-BN was successfully prepared. The catalyst was characterized by FT-IR, SEM, TG, XRD and XPS, and the loading level of Pd in h-BN@β-CD@Pd(II) was measured to be 0.088?mmol g?1 by ICP. It exhibits excellent catalytic activity for the Suzuki and Heck reactions in water, and can be easily separated and consecutively reused for at least nine times. In addition, a series of pharmacologically interesting products were successfully synthesized using this catalyst to demonstrate its potential applications in pharmaceutical industries. Above all, this work opens up an interesting and attractive avenue for the use of cyclodextrin-functionalized h-BN as an efficient support for hydrophilic heterogeneous catalysts.

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.