Sodium ethylxanthogenate
Product Information
Molecular Formula
C3H5NaOS2
Molecular Weight
144.18
Description
Sodium ethylxanthogenate is a prevalent chemical compound within the biomedicine sphere and serves as a fundamental reagent in the synthesis of organic compounds. Its multidimensional potential encompasses the treatment of diverse diseases, including the intricate realm of cancer, as it embodies a pivotal precursor for the evolution of potent anticancer drugs. Moreover, this compound finds extensive utility within the drug discovery framework, perpetuating kinetic advancements in the realm of biomedical research.
Synonyms
SODIUM ETHYL XANTHATE; SODIUM ETHYLXANTHOGENATE; SODIUM O-ETHYL DITHIOCARBONATE; SODIUM XANTHOGENATE; carbonicacid,dithio-,o-ethylester,sodiumsalt; sodium-o-ethylcarbonodithioate; carbonodithioic acid o-ethyl ester sodium salt; ETHYLXANTHIC ACID SODIUM SALT
IUPAC Name
sodiumethoxymethanedithioate
SMILES
CCOC(=S)[S-].[Na+]
InChI
InChI=1S/C3H6OS2.Na/c1-2-4-3(5)6/h2H2,1H3,(H,5,6)/q+1/p-1
InChI Key
RZFBEFUNINJXRQ-UHFFFAOYSA-M
Purity
N/A
Density
1.181g/cm3
Appearance
Light orange to Yellow to Green powder to crystal
Safety Information
Hazards
H302:
Harmful if swallowed.
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Harmful if swallowed.
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Precautionary Statement
P264:
Wash thoroughly after handling.
P270:
Do not eat, drink or smoke when using this product.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P301+P312+P330:
IF SWALLOWED:
Call a POISON CENTER or doctor/physician if you feel unwell.
Rinse mouth.
P337+P313:
If eye irritation persists:
Get medical advice/attention.
P501:
Dispose of contents/container in accordance with local/regional/national/international regulations.
Wash thoroughly after handling.
P270:
Do not eat, drink or smoke when using this product.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P301+P312+P330:
IF SWALLOWED:
Call a POISON CENTER or doctor/physician if you feel unwell.
Rinse mouth.
P337+P313:
If eye irritation persists:
Get medical advice/attention.
P501:
Dispose of contents/container in accordance with local/regional/national/international regulations.
Computed Properties
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
3
Rotatable Bond Count
2
Exact Mass
143.96795141 g/mol
Monoisotopic Mass
143.96795141 g/mol
Topological Polar Surface Area
42.3Ų
Heavy Atom Count
7
Formal Charge
0
Complexity
56.9
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
2
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-114163396-A | Preparation method of epalrestat intermediate | 2021-12-14 |
| CN-113976331-A | Method for preparing high-purity pyrite by flotation mass transfer dynamics regulation | 2021-10-22 |
| CN-113861202-A | Large-scale preparation process of pterosin | 2021-10-14 |
| CN-113831269-A | Synthesis method of vinyl dithiocarbamate compound | 2021-09-25 |
| CN-113893952-A | Copper-cobalt ore beneficiation method | 2021-09-18 |
| CN-113788733-A | Deuterated method of trans-olefin | 2021-08-19 |
| CN-113603892-A | Elastic polymer binder applied to silicon electrode of ion battery and preparation method thereof | 2021-07-27 |
| CN-113480459-A | Preparation method of xanthate alkyl hydroximate | 2021-07-01 |
| CN-113354810-A | Clustering peptide with side chain containing functionalized biphenyl group and preparation method thereof | 2021-06-07 |
| CN-113318855-A | Flotation system and process for improving quality and reducing impurities of high-clay-content low-grade chalcopyrite | 2021-06-02 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 21732640 | 2011-08-19 | Synthesis of unsymmetrical sulfides using ethyl potassium xanthogenate and recyclable copper catalyst under ligand-free conditions | The Journal of organic chemistry |
| 21271689 | 2011-03-04 | Cu-catalyzed one-pot synthesis of unsymmetrical diaryl thioethers by coupling of aryl halides using a thiol precursor | Organic letters |
| 20602971 | 2010-07-15 | Flow injection analysis of ethyl xanthate by gas diffusion and UV detection as CS2 for process monitoring of sulfide ore flotation | Talanta |
| 19534151 | 2009-05-01 | Uptake of hydrophobic metal complexes by three freshwater algae: unexpected influence of pH | Environmental science & technology |
| 14575499 | 2003-10-31 | Use of 13C as an indirect tag in 15N specifically labeled nucleosides. Syntheses of [8-13C-1,7,NH2-15N3]adenosine, -guanosine, and their deoxy analogues | The Journal of organic chemistry |
| 12747729 | 2003-04-01 | Derivatives of xanthic acid are novel antioxidants: application to synaptosomes | Free radical research |
| 12141997 | 2002-09-02 | Integrated copper-containing wastewater treatment using xanthate process | Journal of hazardous materials |
