Dithiolane

Dithiolane

Names
IUPAC name Dithiolane
Other names 1,2-dithiolane, 1,3-dithiolane
Identifiers
3D model (JSmol)	Interactive image
ChEBI	CHEBI:38226 Y
ChemSpider	71377 Y
PubChem CID	79045
InChI InChI=1S/C3H6S2/c1-2-4-5-3-1/h1-3H2 Y Key: MUZIZEZCKKMZRT-UHFFFAOYSA-N Y InChI=1/C3H6S2/c1-2-4-5-3-1/h1-3H2 Key: MUZIZEZCKKMZRT-UHFFFAOYAH
SMILES S1SCCC1
Properties
Chemical formula	C3H6S2
Related compounds
Related compounds	1,2-Ethanedithiol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y  (what is YN ?)
Infobox references

A dithiolane is a sulfur heterocycle derived from cyclopentane by replacing two methylene bridges (-CH
2- units) with thioether groups. The parent compounds are 1,2-dithiolane and 1,3-dithiolane.

1,2-Dithiolanes, such as lipoic acid, are cyclic disulfides.

1,3-Dithiolanes are important as protecting groups for carbonyl compounds, since they are inert to a wide range of conditions. Reacting a carbonyl group with 1,2-ethanedithiol converts it to a 1,3-dithiolane, as detailed below.

A dithiolanone is a dithiolane which is also a ketone.