Sodium ethylxanthogenate

Inquiry

Molecular Formula:

C3H5NaOS2

Molecular Weight:

144.18

CAS Number:

140-90-9

Catalog Number:

140-90-9

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

Canonical 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.

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.

Computed Properties

Hydrogen Bond Donor Count

Hydrogen Bond Acceptor Count

Rotatable Bond Count

Exact Mass

143.96795141 g/mol

Monoisotopic Mass

143.96795141 g/mol

Topological Polar Surface Area

42.3Å²

Heavy Atom Count

Formal Charge

Complexity

56.9

Isotope Atom Count

Defined Atom Stereocenter Count

Undefined Atom Stereocenter Count

Defined Bond Stereocenter Count

Undefined Bond Stereocenter Count

Covalently-Bonded Unit Count

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

The molarity calculator equation

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The dilution calculator equation

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