39213-13-3

Basic information

• Product Name: 1-OXIDE-4-THIOMORPHOLINE
• Synonyms: 1-OXIDE-4-THIOMORPHOLINE;1-OXIDE-4-THIOMORPHOLINE HYDROCHLORIDE;4-THIOMORPHOLINE-1-OXIDE;1-OXIDE THIOMORPHOLINE HYDROCHLORIDE;ThioMorpholine, 1-oxide;4-Thiomorpholin-1-oxide;EOS-62359
• CAS NO: 39213-13-3
• Molecular Formula: C₄H₉NOS
• Molecular Weight: 119.19
• Mol File: 39213-13-3.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 318.322°C at 760 mmHg
• Flash Point: 146.316°C
• Appearance: /
• Density: 1.264g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.572
• CAS DataBase Reference: 1-OXIDE-4-THIOMORPHOLINE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-OXIDE-4-THIOMORPHOLINE(39213-13-3)
• EPA Substance Registry System: 1-OXIDE-4-THIOMORPHOLINE(39213-13-3)

Safety Data

• Hazard Codes: Xi
• Statements: 36
• Safety Statements: 26
• Hazardous Substances Data: 39213-13-3(Hazardous Substances Data)

Usage

Structure

Contains both oxygen and sulfur in its structure, which contributes to its unique properties and reactivity.

Applications

a. Pharmaceutical industry used as an intermediate in the synthesis of other organic compounds.
b. Agrochemicals potential uses in the development of agricultural chemicals.
c. Organic chemistry reactions serves as a reagent in various organic chemistry reactions.

Chemical reactivity

Known for its ability to participate in a wide range of chemical reactions, making it a versatile compound.

Versatility

Capable of forming new chemical bonds, which allows it to be used as a building block in the synthesis of diverse organic compounds.

Industrial significance

1-OXIDE-4-THIOMORPHOLINE is a valuable compound with potential applications in different industrial sectors, including pharmaceuticals, agrochemicals, and organic chemistry.

InChI:InChI=1/C4H9NOS/c6-7-3-1-5-2-4-7/h5H,1-4H2

Upstream product

• 123-90-0 Thiomorpholin 
• 1115-15-7 divinyl sulfoxide 

Downstream Products

• 1454648-68-0 (S)-3-[4-(1-oxo-1λ⁴-thiomorpholin-4-ylmethyl)-phenyl]-2,3-dihydro-[1,4]dioxino[2,3-b]pyridine 
• 1080062-06-1 4-{[6-(5-{1-[4-(cyclopropylsulfonyl)phenyl]-2-(tetrahydro-2H-pyran-4-yl)ethyl}-1H-pyrrol-2-yl)pyridin-3-yl]methyl}thiomorpholine 1-oxide 
• 76176-88-0 N-Ac-1,4-thiazane-1-oxide 
• 80348-41-0 N-(5,5-dimethyl-3-thioxo-2-cyclohexenyl)-perhydro-1,4-thiazine 1-oxide 

Relevant articles and documents

Synthesis, Characterization and Catalytic Activity of a Tungsten(VI) Amino Triphenolate Complex

Abstract: Synthesis, characterization and catalytic activity of a novel tungsten(VI) amino triphenolate complex have been investigated. In particular, a tungsten(VI) amino triphenolate complex has been synthesized and tested in the oxidation of sulfides and cyclooctene, using hydrogen peroxide as terminal oxidant. The catalyst has proved to be air and water tolerant, also showing a good efficiency in terms of yields and selectivity. Moreover, an upgrade of our previous ligand synthesis is herein reported. The new developed procedure allows to obtain the triphenolamine in large scale without the use of chromatography for the intermediates purification. Graphical Abstract: [Figure not available: see fulltext.].

BENZODIOXANE INHIBITORS OF LEUKOTRIENE PRODUCTION FOR COMBINATION THERAPY

The present invention relates to a combination comprising compounds of formula (I): wherein R1 to R3, A, X and n are as defined herein, and an additional active agent. The present invention also relates to pharmaceutical compositions comprising these combinations, and methods of using these combinations to treat various diseases and disorders.

Benzothiazole derivatives with activity as adenosine receptor ligands

The present invention relates to substituted benzothiazole derivitives and to their pharmaceutically acceptable salts useful for the treatment of diseases related to the adenosine receptor.