CAS 83373-60-8
:Potassium O-(octahydro-4,7-methano-1H-inden-5-yl) carbonodithioate (1:1)
Description:
Potassium O-(octahydro-4,7-methano-1H-inden-5-yl) carbonodithioate, with the CAS number 83373-60-8, is a chemical compound that belongs to the class of dithioates. This substance features a potassium cation associated with an anionic dithioate group, which is characterized by the presence of two sulfur atoms bonded to a carbon atom that is also connected to an organic moiety. The organic part of the molecule is derived from octahydro-4,7-methano-1H-inden, indicating a bicyclic structure that is fully saturated, contributing to its stability and potential reactivity. The presence of the dithioate functional group suggests that this compound may exhibit properties typical of thiolates, such as nucleophilicity and the ability to form coordination complexes with metals. Its applications could span various fields, including agriculture as a potential pesticide or fungicide, or in materials science for the development of novel compounds. However, specific safety and handling guidelines should be followed due to the potential reactivity of sulfur-containing compounds.
Formula:C11H15KOS2
InChI:InChI=1/C11H16OS2.K/c13-11(14)12-10-5-6-4-9(10)8-3-1-2-7(6)8;/h6-10H,1-5H2,(H,13,14);
InChI key:InChIKey=YFUFHKMDCZBHMY-UHFFFAOYSA-N
SMILES:O(C(=S)S)C1C2C3C(C(C2)C1)CCC3.[K]
Synonyms:- Carbonodithioic acid, O-(octahydro-4,7-methano-1H-inden-5-yl) ester, potassium salt
- Carbonodithioic acid, O-(octahydro-4,7-methano-1H-inden-5-yl) ester, potassium salt (1:1)
- D 609
- O-(Octahydro-4,7-methano-1H-inden-5-yl)carbonodithioate potassium salt
- O-(octahydro-1H-4,7-methanoinden-5-yl) hydrogen carbonodithioate
- Potassium O-(octahydro-4,7-methano-1H-inden-5-yl) carbonodithioate (1:1)
- Tricyclo-decan-9-yl-xanthate
- Tricyclodecane-9-yl-xanthogenate
- potassium O-(octahydro-1H-4,7-methanoinden-5-yl) dithiocarbonate
- Potassium O-(octahydro-4,7-methano-1H-inden-5-yl) dithiocarbonate
- TRICYCLODECAN-9-YL XANTHOGENATE POTASSIUM SALT
- D609 potassium salt,98%
- CARBONODITHIOIC ACID, O-(OCTAHYDRO-4,7-METHANO-1H-INDEN-5-YL) ESTER POTASSIUM
- O-TRICYCLO(5.2.1.02,6)DEC-9-YL*DITHIOCAR BONATE POTA
- D609
- Tricyclodecan-9-yl xanthate potassium salt
- CARBONODITHIOIC ACID, O-(OCTAHYDRO-4,7-METH
- O-TRICYCLO[5.2.1.0(2,6)]DEC-9-YL DITHIOCARBONATE POTASSIUM SALT
- TRICYCLODECAN-9-YL XANTHOGENATE K
- Dithiocarbonic acid O-[(octahydro-4,7-methano-1H-inden)-5-yl]S-potassium salt
- D-609 POTASSIUM
- D609 POTASSIUM SALT
- Tricyclodecan-9-yl xanthate
- Tricyclodecan-9-yl xanthogenate
- O-(OCTAHYDRO-4,7-METHANO-1H-INDEN-5-YL) CARBONOPOTASSIUM DITHIOATE
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Found 6 products.
Tricyclo-decan-9-yl-xanthate
CAS:Formula:C11H15KOS2Purity:%Color and Shape:SolidMolecular weight:266.4645O-Tricyclo[5.2.1.02,6]dec-9-yl dithiocarbonate potassium salt
CAS:Formula:C11H15KOS2Purity:≥ 98.0%Color and Shape:Off-white to yellow powderMolecular weight:266.46Carbonodithioic Acid O-(Octahydro-4,7-methano-1H-inden-5-yl) Ester Potassium Salt
CAS:Controlled ProductFormula:C11H15KOS2Color and Shape:NeatMolecular weight:266.464O-Tricyclo[5.2.1.02,6]dec-9-yl dithiocarbonate potassium salt
CAS:<p>O-Tricyclo[5.2.1.02,6]dec-9-yl dithiocarbonate potassium salt (OTCDK) is a cytosolic calcium ionophore that activates soluble guanylate cyclase (sGC). This activation leads to an increase in intracellular levels of cGMP and thereby the production of nitric oxide (NO). OTCDK has been shown to inhibit the synthesis of prostanoids by inhibiting the activity of enzymes such as phospholipase A2 and COX-2 that are responsible for the conversion of arachidonic acid to prostaglandins. This drug also inhibits bladder contractility and relaxes muscle, which may be due to its ability to inhibit calcium influx into cells. OTCDK has been shown to induce relaxation in isolated arteries and reduce atherosclerotic lesion size in mice. The concentration-response curve for OTCDK was found to be steepest</p>Formula:C11H15KOS2Purity:Min. 95%Molecular weight:266.46 g/molD609
CAS:D609 (Tricyclodecan-9-yl-Xanthogenate) has antiviral and antiproliferative activities.D609 acts through competitive inhibition of PC, PC-P and SMS.Formula:C11H15KOS2Purity:97.67% - 99.56%Color and Shape:Off-White PowderMolecular weight:266.46





