77129-81-8

Basic information

• Product Name: Ethanethione, 2-(4-broMophenyl)-1-(4-Morpholinyl)-
• Synonyms: Ethanethione, 2-(4-broMophenyl)-1-(4-Morpholinyl)-;2-(4-bromophenyl)-1-(4-morpholinyl)Ethanethione;2-(4-bromophenyl)-1-morpholin-4-ylethanethione
• CAS NO: 77129-81-8
• Molecular Formula: C₁₂H₁₄BrNOS
• Molecular Weight: 300.21466
• Mol File: 77129-81-8.mol
• Article Data: 12

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Ethanethione, 2-(4-broMophenyl)-1-(4-Morpholinyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanethione, 2-(4-broMophenyl)-1-(4-Morpholinyl)-(77129-81-8)
• EPA Substance Registry System: Ethanethione, 2-(4-broMophenyl)-1-(4-Morpholinyl)-(77129-81-8)

Safety Data

• Hazardous Substances Data: 77129-81-8(Hazardous Substances Data)

Usage

General Description

Ethanethione, 2-(4-broMophenyl)-1-(4-Morpholinyl)- is a compound with the chemical formula C11H15BrNOS. It is a thioether compound that contains a bromophenyl group and a morpholinyl group. Thioether compounds are known for their strong odors and often have industrial applications as solvents and reagents. The bromophenyl group is a common aromatic substituent, and the presence of the morpholinyl group suggests potential biological activity. Ethanethione, 2-(4-broMophenyl)-1-(4-Morpholinyl)- may be of interest for further study in pharmaceutical or chemical research due to its unique structure and potential properties.

Upstream product

• 13621-46-0 1-(4-bromophenyl)-2-morpholino-2-thioxoethan-1-one 
• 110-91-8 morpholine 
• 99-90-1 para-bromoacetophenone 

Downstream Products

• 1393898-12-8 4-(4-bromophenyl)-5-(morpholin-4-yl)-3-phenylthiophen-2(3H)-one 
• 13621-46-0 1-(4-bromophenyl)-2-morpholino-2-thioxoethan-1-one 
• 1878-68-8 2-(4-bromophenyl)-acetic acid 
• 159298-76-7 (Z)-2-(4-Bromo-phenyl)-1,3-di-morpholin-4-yl-propenethione 

Relevant articles and documents

Preparation method of phenyl crotonic acid ester compound

The invention relates to the technical field of organic synthesis, in particular to a preparation method of a phenyl crotonate compound, the preparation method comprises the following steps: S1, carrying out Willgerodt-Kindler reaction on an acetophenone

Selective reduction of carbonyl groups in the presence of low-valent titanium reagents

The chemoselective reduction of several structurally diverse compounds containing carbonyl groups was achieved in the presence of low-valent titanium reagents. This novel synthetic method provides easy access to highly selective reduction of carbonyl groups, and possesses several advantages including one-step procedure, convenient manipulation, good to excellent yields, and short reaction times.

Ultrasound-mediated willgerodt-kindler reactions: Non-thermal synthesis of thioacetamides

Non-thermal, solvent-free condensation of several aryl methyl ketones with amines and elemental sulfur is efficiently conducted using ultrasonic irradiation within short time periods. Consequently, various thioacetamides are conveniently synthesized. Simi