4946-13-8

Basic information

• Product Name: 4-ETHYLTHIOPHENOL
• Synonyms: 4-ETHYLBENZENETHIOL;4-ETHYLTHIOPHENOL;4-ETHYLTHIOPHENOL 97%;4-Ethylthiophenol,97%;4-Ethylbenzenethiol, 4-Ethylphenyl mercaptan
• CAS NO: 4946-13-8
• Molecular Formula: C₈H₁₀S
• Molecular Weight: 138.23
• EINECS: -0
• Product Categories: Phenol&Thiophenol&Mercaptan;Phenoles and thiophenoles
• Mol File: 4946-13-8.mol
• Article Data: 7

Chemical Properties

• Melting Point: -30°C (estimate)
• Boiling Point: 119 °C
• Flash Point: 119-120°C/30mm
• Appearance: clear, colorless liquid
• Density: 1.02
• Vapor Pressure: 0.262mmHg at 25°C
• Refractive Index: 1.563
• PKA: 6.84±0.10(Predicted)
• Sensitive: Air Sensitive
• BRN: 1905734
• CAS DataBase Reference: 4-ETHYLTHIOPHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-ETHYLTHIOPHENOL(4946-13-8)
• EPA Substance Registry System: 4-ETHYLTHIOPHENOL(4946-13-8)

Safety Data

• Hazard Codes: Xi
• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36/37/39-36/37-23
• RIDADR: 2810
• HazardClass: 6.1
• Hazardous Substances Data: 4946-13-8(Hazardous Substances Data)

Usage

Uses

4-ETHYLTHIOPHENOL is a useful research chemical.

Chemical Properties

Colorless to pale yellow liquid

InChI:InChI=1/C8H10S/c1-2-7-3-5-8(9)6-4-7/h3-6,9H,2H2,1H3/p-1

Upstream product

• 31218-75-4 (4-ethylphenyl)(methyl)sulfane 
• 589-16-2 4-aminoethylbenzene 
• 65398-58-5 Thiocarbonic acid S-(4-ethyl-phenyl) ester O-methyl ester 
• 16712-69-9 p-ethylbenzenesulfonyl chloride 

Downstream Products

• 79506-63-1 2-((4-ethylphenyl)thio)acetonitrile 
• 91258-51-4 2-(4-Ethyl-phenylsulfanyl)-N-hydroxy-acetamidine 
• 110955-58-3 p-ethylbenzenesulfinyl chloride 
• 956036-90-1 2-amino-2-[2-[4'-(4-ethylphenylthio)-2'-fluorobiphenyl-4-yl]ethyl]propane-1,3-diol 
• 1241768-99-9 C₁₇H₂₀O₂S 
• 102143-23-7 3-((4-ethylphenyl)thio)propanoic acid 
• 16712-69-9 p-ethylbenzenesulfonyl chloride 
• 62248-44-6 (4-ethylphenyl)(4-nitrophenyl)sulfane 
• 1160217-95-7 2-acetamido-3-(4-ethylphenylsulfanyl)propionic acid methyl ester 
• 70931-57-6 2-ethyl-7-fluoro-11-(4-methylpiperazino)-10,11-dihydrodibenzothiepin 
• 172421-70-4 2-p-ethylphenylthiomethyl-3-ethoxycarbonyl-5-hydroxybenzofuran 
• 152027-87-7 1,4-Diazido-2,3-bis-(4-ethyl-phenylsulfanyl)-anthraquinone 

Relevant articles and documents

The Reaction of Alkyl-substituted Thioanisoles with PCl3 and AlCl3: a Route to Benzothiadiphospholobenzothiadiphosphole Derivatives

The synthesis of benzothiadiphospholobenzothiadiphosphole derivatives starting from alkyl-substituted thioanisoles and PCl3-AlCl3 is reported.The reaction is carried out at reflux in the absence of solvent and the yields are dependent on the starting sulphide.These new heterocycles can be purified by simple filtration on a Florisil column and have been characterized by 1H-, 13C-, (1H)31P-n.m.r. and mass spectroscopy analyses.New unexpected findings are also described.

MOESSBAUER AND NUCLEAR MAGNETIC RESONANCE SPECTROSCOPIC STUDIES ON 'MYOCRISIN', 'SOLGANOL', 'AURANOFIN', AND RELATED GOLD(I) THIOLATES

A large number of gold(I) thiolates, , have been prepared in which the R group is an alkyl, aryl, carboxylic acid, amino acid, or heterocycle.Most are highly insoluble in all common solvents, but (R' = Et, iPr, sBu, or tBu) dissolv

Antiallergic cyclic sulphur compounds

Certain tricyclic thioxanthone-10,10-dioxide compounds each of which is substituted in the 1-,2-,3- or 4-position by a carboxyl or (5-tetrazolyl) group and each of which is optionally substituted in the 5-,6-,7- or 8-position by a second carboxyl or (5-tetrazolyl) group or a substituent selected from cyano, halogen, nitro, alkyl, alkoxy, acyl, amino, acylamino, thioalkyl, alkylsulphinyl and alkylsulphonyl, as well as salts, and optionally substituted esters and amides of the carboxyl substituted compounds and alkyl derivatives of the tetrazolyl substituted compounds, are useful for the relief or prophylaxis of allergic conditions.