Potassium ethyl xanthogenate - ≥98% , CAS No.140-89-6

CAS: 140-89-6 Cat. No.: P111000 Formula: C₃H₅KOS₂ Peso molecolare: 160.3 Beilstein Registry Number: 3596974 Numero EC: 205-439-3

GRADE & PURITY ≥98%

Synonyms

C3H5KOS2 | EC 205-439-3 | Kaliumxanthogenat | Potassium ethyl xanthogenate, 97% | DTXCID4022315 | BDBM50004940 | ethoxy(potassiosulfanyl)methanethione | Ethyl potassium xanthate | D78138 | E0194 | Z 3 (VAN) | JCBJVAJGLKENNC-UHFFFAOYSA-M | FT-0651308 | POT

Storage

Room temperature

Shipped In

Normal

Panoramica

Potassium ethyl xanthogenate (ethyl potassium xanthogenate) has been used: in synthesis of unsymmetrical sulfides via cross-coupling reaction, using recyclable CuO nanoparticles under ligand-free conditions as surfactant to investigate the adsorption of colloidal dye Disperse Blue 3 onto pretreated polyester fabric in determination of microgram amounts of cadmium in water samples by substoichiometric radiochemical method

Specifications

Sinonimi

C3H5KOS2 | EC 205-439-3 | Kaliumxanthogenat | Potassium ethyl xanthogenate, 97% | DTXCID4022315 | BDBM50004940 | ethoxy(potassiosulfanyl)methanethione | Ethyl potassium xanthate | D78138 | E0194 | Z 3 (VAN) | JCBJVAJGLKENNC-UHFFFAOYSA-M | FT-0651308 | POT

Specifiche e purezza

≥98%

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

Normal

Purezza

≥98%

Nomi e identificatori

Pubchem Sid

504761237

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504761237

Sorrisi canonici

CCOC(=S)[S-].[K+]

IUPAC Name

potassium;ethoxymethanedithioate

InChIKey

JCBJVAJGLKENNC-UHFFFAOYSA-M

INCHI

1S/C3H6OS2.K/c1-2-4-3(5)6;/h2H2,1H3,(H,5,6);/q;+1/p-1

Isomeri SMILES

CCOC(=S)[S-].[K+]

WGK Germania

3

RTECS

FG1575000

CAS alternativo

151-01-9

Numero UN

3342

Gruppo di imballaggio

II

Peso molecolare

160.3

Beilstein

3596974

Reaxy-Rn

3596974

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3596974&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic salts
    • Classe Organic metal salts
      • Subclass Organic alkali metal salts

• Kingdom: Organic compounds
• Superclass: Organic salts
• Classe: Organic metal salts
• Subclass: Organic alkali metal salts
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic alkali metal salts
• Alternative Parents: Organosulfur compounds Organooxygen compounds Organic potassium salts Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organic alkali metal salt - Organic oxygen compound - Hydrocarbon derivative - Organic potassium salt - Organosulfur compound - Organooxygen compound - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as organic alkali metal salts. These are organic salts of an alkali metal. The alkali metal atom is usually in its ionic form.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Obiettivi associati (umani)

CA1 Tclin Carbonic anhydrase 1 (1 Activities)

Discover Target: CA1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA2 Tclin Carbonic anhydrase 2 (1 Activities)

Discover Target: CA2

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA12 Tclin Carbonic anhydrase 12 (1 Activities)

Discover Target: CA12

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA9 Tclin Carbonic anhydrase 9 (1 Activities)

Discover Target: CA9

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA2 Tclin Carbonic anhydrase II (17698 Activities)

Discover Target: CA2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA1 Tclin Carbonic anhydrase I (13240 Activities)

Discover Target: CA1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA12 Tclin Carbonic anhydrase XII (6231 Activities)

Discover Target: CA12

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Water: very soluble(lit.) Aalcohol: soluble(lit.)
• Sensibilità: light sensitive,Moisture sensitive.
• Punto di infiammabilità (°F): 204.8 °F
• Punto di infiammabilità (°C): 96 °C
• Punto di fusione (°C): 210°C
• Peso molecolare: 160.300 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 159.942 Da
• Monoisotopic Mass: 159.942 Da
• Topological Polar Surface Area: 42.300 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 56.900
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

XLogP3