6325-92-4

Basic information

• Product Name: 2-(benzylthio)aniline
• CAS NO: 6325-92-4
• Molecular Formula: C₁₃H₁₃NS
• Molecular Weight: 390.3639
• EINECS: 228-690-0
• Mol File: 6325-92-4.mol
• Article Data: 22

Chemical Properties

• Boiling Point: 487.1°C at 760 mmHg
• Flash Point: 248.4°C
• Density: 1.41g/cm³
• Vapor Pressure: 1.22E-09mmHg at 25°C
• Refractive Index: 1.678
• CAS DataBase Reference: 2-(benzylthio)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(benzylthio)aniline(6325-92-4)
• EPA Substance Registry System: 2-(benzylthio)aniline(6325-92-4)

Safety Data

• Hazardous Substances Data: 6325-92-4(Hazardous Substances Data)

Usage

General Description

2-(Benzylthio)aniline is a chemical compound with the molecular formula C13H13NS. It is a yellowish to light brown solid with a molecular weight of 211.31 g/mol. 2-(Benzylthio)aniline is a thioaniline, meaning it contains a sulfur atom attached to an aniline group. It is used in the synthesis of various organic compounds, such as dyes, pharmaceuticals, and agrochemicals. 2-(Benzylthio)aniline is also known to exhibit biological properties, including antibacterial and antifungal activities. It is important to handle this chemical with care, as it can be hazardous if not properly managed.

Upstream product

• 100-44-7 benzyl chloride 
• 137-07-5 2-amino-benzenethiol 
• 615-43-0 2-iodophenylamine 
• 100-53-8 phenylmethanethiol 
• 1493-27-2 ortho-nitrofluorobenzene 
• 1421772-90-8 2-(benzylthio)-N-{pyridin-4-ylmethylidene}aniline 
• 100-39-0 benzyl bromide 
• 105903-46-6 S-benzyl ortho-aminothiophenol hydrochloride 
• 4875-10-9 o-nitrothiophenol 
• 1408300-21-9 2-amino-S-cinnamylthiophenol 
• 77053-20-4 2-(2-propen-1-ylsulfanyl)aniline 
• 615-36-1 2-bromoaniline 
• 22057-44-9 1-(benzylsulfanyl)-2-nitrobenzene 

Downstream Products

• 91435-60-8 2-benzylthio-N-benzylideneaniline 
• 107344-52-5 1-(2-benzylthiophenyl)pyrrole 
• 5325-20-2 2H-1,4-benzothiazin-3-one 
• 137411-41-7 3-(2-Benzylsulphinylanilino)-5,5-dimethylcyclohex-2-enone 
• 137411-48-4 5-benzyl 1,2,3,4-tetrahydro-2,2-dimethyl-4-oxo-10H-phenothiazin-5-ium picrate 
• 105903-46-6 S-benzyl ortho-aminothiophenol hydrochloride 
• 1196988-03-0 N-(2-benzylsulfanylphenyl)-2-bromobenzenesulfonamide 
• 1222172-75-9 [Pt(2-(N-benzyl)amidothiphenolate)(2-(phenylazo)pyridine)] 
• 1421772-90-8 2-(benzylthio)-N-{pyridin-4-ylmethylidene}aniline 
• 1428670-61-4 3-((2-(benzylthio)phenylimino)methyl)-2-hydroxy-5-methylbenzaldehyde 
• 142913-02-8 2-((2-(benzylthio)phenylimino)methyl)phenol 
• 614734-69-9 benzo[b]thiophene-2-carboxylic acid (2-benzylsulfanyl-phenyl)-(3-methylamino-propyl)-amide 

Relevant articles and documents

2-benzylthio-aniline croconic acid cyanine chemical sensor capable of identifying Hg and preparation method of chemical sensor

The invention relates to a 2-benzylthio-aniline croconic acid cyanine chemical sensor capable of identifying Hg and a preparation method of the chemical sensor. The preparation method comprises steps as follows: 2-benzylthio-aniline is synthesized from 2-aminothiophenol and benzyl chloride, and a 2-benzylthio-aniline croconic acid cyanine dye compound is synthesized from 2-benzylthio-aniline and croconic acid. The chemical sensor and the preparation method have beneficial effects as follows: the synthetic process is relatively simple, reaction conditions are easy to control, and the prepared 2-benzylthio-aniline croconic acid cyanine dye has excellent optical performance and optical stability. When the 2-benzylthio-aniline croconic acid cyanine dye is used for identifying Hg, colorof a solution also changes besides change of an absorption spectrum, so that the 2-benzylthio-aniline croconic acid cyanine dye has a colorimetric identification function and facilitates detection for Hg. Besides, the 2-benzylthio-aniline croconic acid cyanine dye has good selectivity and anti-interference performance for identification of Hg.

Palladium nanoparticles stabilized by aqueous vesicles self-assembled from a PEGylated surfactant ionic liquid for the chemoselective reduction of nitroarenes

Vesicles self-assembled from an aqueous PEGylated surfactant ionic liquid solution can be applied for stabilizing palladium nanoparticles, which prove to be an efficient catalytic system for chemoselective hydrogen transfer of nitroarenes using hydrazine hydrate as a hydrogen source. The particle sizes of vesicles are decreased with the increase of ionic liquid's concentrations and relatively small particle sizes are beneficial to the reduction. Moreover, the aqueous catalytic system still stays in reactor by simple extraction, and is reused without further treatment.

Eco-compatible three component strategies for C-S bond formation in thioether and S-aryl-carbamodithioate compounds catalyzed by copper(II) nanoparticles supported on modified AlPO4

One-pot and three components C-S bond formation reactions in thioethers and S-aryl-carbamodithioates have been catalyzed by a copper heterogeneous nano-catalyst supported on modified AlPO4 under different reaction conditions. The above-mentioned nano-catalyst has been characterized by various techniques such as SEM, TEM, AFM, XRD, FT-IR, UV–Vis, CV, BET, TGA, ICP and XPS spectrometry and its particle size was estimated to be between 60–110?nm. Finally, the reusability of the catalyst up to ten cycles without any significant leaching is one of the outstanding properties of the catalyst.