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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1,4,8,11-Tetrathiacyclotetradecane

C1CSCCSCCCSCCSC1 Request for Quotation
Chemical Name: 1,4,8,11-Tetrathiacyclotetradecane
CAS Number: 24194-61-4
Product Number: AG003DM5(AGN-PC-0JOLWY)
Synonyms:
MDL No:
Molecular Formula: C10H20S4
Molecular Weight: 268.5258

Identification/Properties

Properties
MP:
123 °C
BP:
431.6 °C at 760 mmHg
Form:
Solid
Computed Properties
Molecular Weight:
268.51g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
268.045g/mol
Monoisotopic Mass:
268.045g/mol
Topological Polar Surface Area:
101A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
92.7
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:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,4,8,11-Tetrathiacyclotetradecane, also known as Tetrathiaadamantane, is a unique and versatile compound widely utilized in chemical synthesis processes. This cyclic sulfur compound plays a crucial role in various reactions due to its distinctive structural properties and reactivity.Tetrathiaadamantane is commonly employed as a building block in the synthesis of complex organic molecules, particularly in the formation of sulfur-containing frameworks. Its rigid and symmetrical structure offers a platform for the creation of novel molecular architectures with specific functionalities. Additionally, its sulfur atoms provide sites for various chemical modifications and functional group manipulations, making it a valuable precursor in organic synthesis.In the field of coordination chemistry, 1,4,8,11-Tetrathiacyclotetradecane serves as a ligand in metal complexation reactions due to its ability to chelate metal ions effectively. This property enables the formation of stable metal complexes, which find applications in catalysis, sensing, and material science.Moreover, Tetrathiaadamantane is utilized as a sulfur-rich source in the preparation of sulfur-containing polymers and materials. Its incorporation into polymeric structures imparts unique properties such as enhanced mechanical strength, thermal stability, and chemical resistance.Overall, the versatility and reactivity of 1,4,8,11-Tetrathiacyclotetradecane make it a valuable component in chemical synthesis, enabling the creation of diverse molecules and materials with tailored properties for various applications.