1783-82-0

Basic information

• Product Name: 3-ethylsulfanylaniline
• Synonyms: 3-ethylsulfanylaniline;3-(ETHYLTHIO)ANILINE
• CAS NO: 1783-82-0
• Molecular Formula: C₈H₁₁NS
• Molecular Weight: 153.24
• Mol File: 1783-82-0.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 278.8°Cat760mmHg
• Flash Point: 122.4°C
• Appearance: /
• Density: 1.09g/cm³
• Vapor Pressure: 0.00418mmHg at 25°C
• Refractive Index: 1.594
• PKA: 3.95±0.10(Predicted)
• CAS DataBase Reference: 3-ethylsulfanylaniline(CAS DataBase Reference)
• NIST Chemistry Reference: 3-ethylsulfanylaniline(1783-82-0)
• EPA Substance Registry System: 3-ethylsulfanylaniline(1783-82-0)

Safety Data

• Hazardous Substances Data: 1783-82-0(Hazardous Substances Data)

Usage

General Description

3-ethylsulfanylaniline is a chemical compound with the molecular formula C8H11NS. It is a derivative of aniline, with an ethyl group and a sulfanyl group attached to the aromatic ring. 3-ethylsulfanylaniline is part of a class of organic compounds known as sulfanylbenzenes, which are commonly used in the synthesis of pharmaceuticals, dyes, and other organic chemicals. 3-ethylsulfanylaniline is typically used as an intermediate in the production of various organic compounds and may also have some industrial applications. It is important to handle this chemical with care and follow proper safety protocols, as it may be toxic if ingested or inhaled and can cause irritation to the skin and eyes upon contact.

InChI:InChI=1/C8H11NS/c1-2-10-8-5-3-4-7(9)6-8/h3-6H,2,9H2,1H3

Upstream product

• 22948-02-3 3-aminothiophenol 
• 75-03-6 ethyl iodide 
• 60-29-7 diethyl ether 
• 34126-43-7 ethyl 3-nitrophenylthioether 

Downstream Products

• 83164-93-6 3-Aminophenyl-aethylsulfon 
• 57947-04-3 N-(3-Ethanesulfonyl-phenyl)-C,C,C-trifluoro-methanesulfonamide 
• 57947-03-2 N-(3-Ethanesulfinyl-phenyl)-C,C,C-trifluoro-methanesulfonamide 
• 57946-80-2 N-(3-Ethylsulfanyl-phenyl)-C,C,C-trifluoro-methanesulfonamide 

Relevant articles and documents

AMINATION AND HYDROXYLATION OF ARYLMETAL COMPOUNDS

In one aspect, the present disclosure provides methods of preparing a primary or secondary amine and hydroxylated aromatic compounds. In some embodiments, the aromatic compound may be unsubstituted, substituted, or contain one or more heteroatoms within the rings of the aromatic compound. The methods described herein may be carried out without the need for transition metal catalysts or harsh reaction conditions.

TRPV4 ANTAGONISTS

The present invention relates to quinoline analogs, pharmaceutical compositions containing them and their use as TRPV4 antagonists.

PROTON PUMP INHIBITORS

A proton pump inhibitor containing a compound represented by the formula (I) wherein X and Y are the same or different and each is a bond or a spacer having 1 to 20 carbon atoms in the main chain, R1 is an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group, R2, R3 and R4 are the same or different and each is a hydrogen atom, an optionally substituted hydrocarbon group, an optionally substituted thienyl group, an optionally substituted benzo[b]thienyl group, an optionally substituted furyl group, an optionally substituted pyridyl group, an optionally substituted pyrazolyl group, an optionally substituted pyrimidinyl group, an acyl group, a halogen atom, a cyano group or a nitro group, R5 and R6 are the same or different and each is a hydrogen atom or an optionally substituted hydrocarbon group, which has a superior proton pump action and shows an antiulcer activity and the like after conversion to a proton pump inhibitor in the body, or a salt thereof. or a prodrug thereof is provided.