Cyclooctasulfur

Cyclooctasulfur
Compound Structure:
Synonyms: Cyclic octaatomic sulfur; Cyclooctasulfane; Cyclooctasulfur; Cyclic sulfur S8; Octasulfur; Octasulfur - $-alpha; Octathiocane; Orthorhombic sulfur; Sulfur, mol. (S8); Sulfur octamer; Sulfur pieces, Puratronic; Sulfur powder; Sulfur powder, -325 mesh; Sulp
Compound ID: NMPC-929
PubChem ID:

66348

Molecular Formula: S8
Canonical SMILES: S1SSSSSSS1
InChIKey: JLQNHALFVCURHW-UHFFFAOYSA-N
About the compound:

Cyclooctasulfur is a homomonocyclic compound composed of eight sulfur atoms. It has been isolated from Ganoderma lucidum, a mushroom commonly used in Chinese medicine. It has a role as a fungal metabolite and a bacterial metabolite. It is an elemental sulfur and a homomonocyclic compound. Sulfur is a chemical element that is present in all living tissues. The most commonly used form of pharmaceutical sulfur is Octasulfur (S8). After calcium and phosphorus, it is the third most abundant mineral in the human body. Sulfur is also found in garlic, onions and broccoli. People take sulfur by mouth for shortness of breath, allergies, swelling in the back of the throat (pharyngitis), high cholesterol, clogged arteries, menopause, and upper respiratory tract infections like the common cold. Sulfur seems to have an antibacterial activity. It has been also used for acne.

GHS Hazard Statements

Not Classified

Reported as not meeting GHS hazard criteria by 6 of 6 companies. For more detailed information, please visit ECHA C&L website.


Properties:

Chemical and Physical Properties

Property Name

Property Value

Molecular Weight

256.5 g/mol

XLogP3-AA

3.5

Hydrogen Bond Donor Count

0

Hydrogen Bond Acceptor Count

8

Rotatable Bond Count

0

Exact Mass

255.7765694 g/mol

Monoisotopic Mass

255.7765694 g/mol

Topological Polar Surface Area

202Ų

Heavy Atom Count

8

Formal Charge

0

Complexity

24

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

Source: PubChem

Source Species: Ficus exasperata
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