62604-08-4

Basic information

• Product Name: Methyl morpholine-4-carbodithioate
• Synonyms: Methyl morpholine-4-carbodithioate;methyl 4-morpholinecarbodithioate
• CAS NO: 62604-08-4
• Molecular Formula: C₆H₁₁NOS₂
• Molecular Weight: 177.29
• Mol File: 62604-08-4.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 269.5°C at 760 mmHg
• Flash Point: 116.8°C
• Appearance: /
• Density: 1.251g/cm³
• Vapor Pressure: 0.00722mmHg at 25°C
• Refractive Index: 1.594
• CAS DataBase Reference: Methyl morpholine-4-carbodithioate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl morpholine-4-carbodithioate(62604-08-4)
• EPA Substance Registry System: Methyl morpholine-4-carbodithioate(62604-08-4)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 62604-08-4(Hazardous Substances Data)

Usage

General Description

Methyl morpholine-4-carbodithioate, also known as MMTC, is a chemical compound that belongs to the carbodithioate family. It is a white crystalline substance with a distinct sulfur-like odor and is often used as a fungicide in agricultural and industrial settings. MMTC has shown effectiveness in controlling the growth of various fungi, especially those that affect crops. It is also used in the manufacturing of rubber, plastics, and textiles. However, it is important to handle MMTC with caution as it can be harmful if inhaled, ingested, or comes into contact with skin or eyes. Overall, Methyl morpholine-4-carbodithioate has found important applications in agriculture and industrial processes, but its potential risks should be carefully managed.

InChI:InChI=1/C6H11NOS2/c1-10-6(9)7-2-4-8-5-3-7/h2-5H2,1H3

Upstream product

• 74-88-4 methyl iodide 
• 110-91-8 morpholine 
• 75-15-0 carbon disulfide 
• 23336-68-7 triethylammonium-2-N-morpholino-dithiocarbamate 
• 74734-11-5 1H-imidazole-1-carbodithioic acid methyl ester 
• 873-58-5 sodium N-morpholinocarbamodithioate 
• 77-78-1 dimethyl sulfate 
• 10316-00-4 4-benzyl-morpholine 
• 109-02-4 4-methyl-morpholine 

Downstream Products

• 1403458-34-3 8-[(2R)-(1-(3,5-difluorophenyl)pyrrolidin-2-yl)]-6-(4-methylpiperazine-1-carbonyl)-2-morpholino-4H-chromen-4-one 
• 1403458-71-8 methyl 8-[(2R)-(1-(3-fluorophenyl)pyrrolidin-2-yl)]-2-morpholino-4-oxo-4H-chromene-6-carboxylate 
• 1421044-88-3 8-[(2R)-1-(3-fluorophenyl)pyrrolidin-2-yl]-2-morpholino-4-oxo-4H-chromene-6-carboxylic acid 
• 1403458-66-1 8-[(2R)-(1-(3,5-difluorophenyl)pyrrolidin-2-yl)]-2-morpholino-4-oxo-4H-chromene-6-carboxylic acid 
• 1403458-65-0 methyl 8-[(2R)-1-(3,5-difluorophenyl)pyrrolidin-2-yl]-2-morpholino-4-oxo-chromene-6-carboxylate 
• 1403458-33-2 6-(azetidine-1-carbonyl)-8-[(2R)-(1-(3-fluorophenyl)pyrrolidin-2-yl)]-2-morpholino-4H-chromen-4-one 
• 1403458-32-1 8-[(2R)-(1-(3-fluorophenyl)pyrrolidin-2-yl)]-6-(morpholine-4-carbonyl)-2-morpholino-4H-chromen-4-one 
• 1403458-31-0 8-[(2R)-(1-(3-fluorophenyl)pyrrolidin-2-yl)]-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide 
• 1403458-30-9 6-(azetidine-1-carbonyl)-8-[(2R)-(1-(3,5-difluorophenyl)pyrrolidin-2-yl)]-2-morpholino-4H-chromen-4-one 
• 1403458-27-4 8-[(2S)-1-(3,5-difluorophenyl)pyrrolidin-2-yl]-6-(morpholine-4-carbonyl)-2-morpholino-4H-chromen-4-one 
• 1403458-28-5 8-[(2R)-1-(3,5-difluorophenyl)pyrrolidin-2-yl]-6-(morpholine-4-carbonyl)-2-morpholino-4H-chromen-4-one 
• 1403458-37-6 8-(1-(4-fluorophenyl)pyrrolidin-2-yl)-6-(morpholine-4-carbonyl)-2-morpholino-4H-chromen-4-one 
• 1403458-29-6 8-[1-(3,5-difluorophenyl)pyrrolidin-2-yl]-2-morpholino-6-[(1-oxidothiomorpholin-4-yl)carbonyl]-4H-chromen-4-one 
• 1403458-24-1 8-(1-(3,5-difluorophenyl)pyrrolidin-2-yl)-N-(2-hydroxyethyl)-N-methyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide 

Relevant articles and documents

Synthesis, characterization and evaluation of biological activity of palladium (II) and platinum (II) complexes with dithiocarbamic acids and their derivatives as ligands

We report the preparation and characterization of new complexes of palladium (II) and platinum (II) with some heterocyclic containing dithiocarbamate ligands, such as piperidine-, morpholine-, and thiomorpholine-dithiocarbamate, their methyl esters and the corresponding thiouramdisulphides. These compounds have been studied through spectroscopic techniques, IR spectra, and electronic spectra, thermogravimetric and conductivity measurements. Thermal decomposition of the complexes takes place through a multi-step process involving pyrolysis of the organic moiety that leads to palladium oxide and platinum sponge respectively. All the complexes have been tested for cytostatic activity on KB cells and the most effective compounds also against L1210 and P388 cells.

CHROMENONE COMPOUNDS AS PI 3 -KINASE INHIBITORS FOR THE TREATMENT OF CANCER

The invention concerns chromenone compounds of Formula I; or pharmaceutically-acceptable salts thereof, wherein each of R1, R2, R3, R4, R5, n and R6 has any of the meanings defined hereinbe

CHROMENONE DERIVATIVES

The invention concerns chromenone derivatives of Formula I or a pharmaceutically-acceptable salts thereof, wherein each of R1, R2, R3, R4, R5, R6, R7, R8, n and R9 has any of the meanings defined hereinbefore in the description; processes for their preparation, pharmaceutical compositions containing them and their use in the manufacture of a medicament for use in the treatment of cell proliferative disorders.