CSC1=NC(C)(\C=C2\N\C(CC2(C)C)=C(\SCC(=O)SC(C)(C)C)C(=O)SC(C)(C)C)C(C)(C)C1

InChIKey=YIBQMWDSYDZDLV-VHVRRWJNSA-N

C27H44N2O2S4

556.9

Organic compounds

Organosulfur compounds

Imidothioesters

Imidothiolactones

Not available

Imidothiolactones

Vinylogous amides Pyrrolines Pyrrolidines Thioesters Thioenol ethers Carbothioic S-esters Sulfenyl compounds Propargyl-type 1,3-dipolar organic compounds Enamines Dialkylamines Carboxylic acids and derivatives Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aliphatic heteromonocyclic compounds

Imidothiolactone - Pyrrolidine - Pyrroline - Vinylogous amide - Thiocarboxylic acid ester - Thioenolether - Carbothioic s-ester - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Secondary aliphatic amine - Enamine - Thiocarboxylic acid or derivatives - Sulfenyl compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic oxygen compound - Hydrocarbon derivative - Amine - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Carbonyl group - Organic oxide - Aliphatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as imidothiolactones. These are analogs of imidolactones where the oxygen atom is replaced by a sulfur atom. They have the general structure RC(=N)SR' where the central carbon atom is part of a ring. R,R' = organyl group.

Not available