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ChemicalBook--->CAS DataBase List--->6573-11-1

6573-11-1

6573-11-1 Structure

6573-11-1 Structure
IdentificationBack Directory
[Name]

1,4,7-TRITHIACYCLONONANE
[CAS]

6573-11-1
[Synonyms]

[9]aneS3
1,4,7-trithionane
TRIETHYLENE TRISULFIDE
1,4,7-TRITHIACYCLONONANE
Hexahydro-1,4,7-trithionin
1,4,7-Trithiacyclononane 97%
1,4,7-TRITHIACYCLONONANE ISO 9001:2015 REACH
1,4,7-Trithiacyclononane,Triethylene trisulfide
[Molecular Formula]

C6H12S3
[MDL Number]

MFCD00010859
[MOL File]

6573-11-1.mol
[Molecular Weight]

180.35
Chemical PropertiesBack Directory
[Melting point ]

78-81 °C(lit.)
[Boiling point ]

79-80 °C
[density ]

1.140±0.06 g/cm3(Predicted)
[BRN ]

1616445
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
[HS Code ]

2934.99.9001
Hazard InformationBack Directory
[Uses]

1,4,7-Trithiacyclononane (9S3) is a tridentate thioether ligand that can be used to prepare complexes with a wide variety of transition metal ions. These complexes often possess exceptional electronic and redox properties. 9S3 ligand reacts with palladium metal ion to form palladium(II) thioether complex, which is used as a catalyst in the C-H activation reactions. Manganese complex of 9S3 ligand is employed as a catalyst for the oxidation of olefins, alkanes, and alcohols.
[Definition]

ChEBI: 1,4,7-trithionane is a crown thioether that is cyclononane in which the carbon atoms at positions 1, 4 and 7 are replaced by sulfur atoms. It is a tridentate thioether ligand that is used to synthesise complexes with a wide variety of transition metal ions. It has a role as a chelator. It is a saturated organic heteromonocyclic parent and a crown thioether.
Spectrum DetailBack Directory
[Spectrum Detail]

1,4,7-TRITHIACYCLONONANE(6573-11-1)1HNMR
1,4,7-TRITHIACYCLONONANE(6573-11-1)Raman
1,4,7-TRITHIACYCLONONANE(6573-11-1)IR
1,4,7-TRITHIACYCLONONANE(6573-11-1)FT-IR
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