13290-16-9

Basic information

• Product Name: 2-(P-TOLYLTHIO)-ETHANOL
• Synonyms: 2-[(4-Methylphenyl)thio]ethanol;Ai3-36461;Ethanol, 2-((4-methylphenyl)thio)-;2-(4-methylphenyl)sulfanylethanol
• CAS NO: 13290-16-9
• Molecular Formula: C₉H₁₂OS
• Molecular Weight: 168.25939
• Mol File: 13290-16-9.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 282°Cat760mmHg
• Flash Point: 137.6°C
• Appearance: /
• Density: 1.11g/cm³
• Vapor Pressure: 0.00163mmHg at 25°C
• Refractive Index: 1.581
• CAS DataBase Reference: 2-(P-TOLYLTHIO)-ETHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(P-TOLYLTHIO)-ETHANOL(13290-16-9)
• EPA Substance Registry System: 2-(P-TOLYLTHIO)-ETHANOL(13290-16-9)

Safety Data

• Hazardous Substances Data: 13290-16-9(Hazardous Substances Data)

Usage

General Description

2-(p-tolylthio)-ethanol, also known as p-tolylthioethanol, is a chemical compound with the molecular formula C9H12OS. It is a clear, colorless to pale yellow liquid with a faint odor. The compound is used as an intermediate in the production of various pharmaceuticals, agrochemicals, and other organic compounds. It is also used as a solvent in various chemical reactions and industrial processes. P-tolylthioethanol has both thiol and hydroxyl functional groups, making it useful in synthetic organic chemistry for building more complex molecules. It is considered to be a hazardous chemical and should be handled and stored with appropriate safety precautions.

InChI:InChI=1/C9H12OS/c1-8-2-4-9(5-3-8)11-7-6-10/h2-5,10H,6-7H2,1H3

Upstream product

• 624-31-7 4-tolyl iodide 
• 60-24-2 2-hydroxyethanethiol 
• 87943-26-8 2-hydroxyethyl p-tolyl sulfoxide 
• 106-45-6 para-thiocresol 
• 540-51-2 2-bromoethanol 
• 106-38-7 para-bromotoluene 
• 107-07-3 2-chloro-ethanol 
• 96991-48-9 3-<2-(4-methylphenyl)-thioethyl>-sydnone 
• 75-21-8 oxirane 

Downstream Products

• 22381-53-9 2-chloroethyl-p-toluenesulfonate 
• 20761-71-1 (2-chloro-ethyl)-p-tolyl sulfide 
• 22381-54-0 2-(p-tolylsulfonyl)ethanol 
• 87943-26-8 2-hydroxyethyl p-tolyl sulfoxide 
• 93008-94-7 N-2-p-Tolylthioaethoxycarbonyl-anilin 
• 106-45-6 para-thiocresol 
• 100059-62-9 [2-(toluene-4-sulfonyl)-ethylsulfanyl]-acetic acid 
• 1390645-77-8 C₁₃H₁₇NO₄S₃ 
• 1390645-74-5 S-2-aminoethyl 2-(2-tosylethylsulfonyl)ethanethioate 
• 1390645-71-2 C₁₃H₁₇NO₅S₂ 
• 1390645-68-7 N-(2-chloroethyl)-2-(4-methylphenylsulfonylethylsulfonyl)acetamide 
• 1390645-65-4 N-(2-hydroxyethyl)-2-(4-methylphenylsulfonylethylsulfonyl)acetamide 
• 1377727-85-9 methyl 2-(2-tosylethylsulfonyl)acetate 
• 1374025-03-2 C₁₁H₁₄O₆S₂ 

Relevant articles and documents

SINGLE-STEP SYNTHESIS METHOD OF ARYL THIOL AND APPLICATION THEREOF

The present invention relates to a single-step synthesis method of aryl thiol, and more specifically, to a method of synthesizing aryl thiol in a single-step by making aryl halide react with alkane dithiol in the presence of a transition metal catalyst. According to the present invention, a single-step synthesis method using the transition metal catalyst, the synthesis method which is capable of synthesizing aryl thiol from aryl halide at a high yield, can be provided. Various aryl halides may be applied to the synthesis method. Further, the synthesis method has advantages that an easily usable reagent may be used, operations are simple, and reactions can be performed under mild conditions. In addition, the synthesized aryl thiol may be used in the synthesis of advanced molecules such as diaryl sulfides and benzothiophenes.COPYRIGHT KIPO 2017

A novel method for the reduction of sulfoxides with the N, N, N g, N g-tetrabromobenzene-1,3-disulfonamide (TBBDA)/PPh3 system

A new method is described for the reduction of sulfoxides to sulfides using N,N,N',N'-tetrabromobenzene-1,3-disulfonamide [TBBDA] in combination with triphenylphosphine. Good to excellent yields, short reaction times, high efficiency and facile isolation of the desired products are the advantages of this method.