CC.CCC1=CC(CC)=CC(CC)=C1.CCC(C)(CC(CC(C)(C)C(=O)OCC=C)C(=O)OC)C(=O)OC.CCC(C)(SC(=S)N(C)C)C(=O)OCCC[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C

InChIKey=DTHIRQJCVBHIGZ-UHFFFAOYSA-N

C50H95NO10S2Si3

1018.68

Organic compounds

Organometallic compounds

Organometalloid compounds

Organosilicon compounds

Not available

Siloxanes

Tricarboxylic acids and derivatives Fatty acid esters Benzene and substituted derivatives Aromatic hydrocarbons Trialkylheterosilanes Dithiocarbamic acid esters Methyl esters Sulfenyl compounds Organic metalloid salts Organonitrogen compounds Hydrocarbon derivatives Organopnictogen compounds Carbonyl compounds Unsaturated hydrocarbons Organic oxides Saturated hydrocarbons

Not available

Siloxane - Tricarboxylic acid or derivatives - Fatty acid ester - Monocyclic benzene moiety - Fatty acyl - Benzenoid - Trialkylheterosilane - Aromatic hydrocarbon - Methyl ester - Dithiocarbamic acid ester - Carboxylic acid ester - Carboxylic acid derivative - Organoheterosilane - Sulfenyl compound - Organic metalloid salt - Organic nitrogen compound - Carbonyl group - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Unsaturated hydrocarbon - Organopnictogen compound - Saturated hydrocarbon - Hydrocarbon - Aromatic homomonocyclic compound

This compound belongs to the class of organic compounds known as siloxanes. These are saturated silicon-oxygen hydrides with unbranched or branched chains of alternating silicon and oxygen atoms (each silicon atom is separated from its nearest silicon neighbours by single oxygen atoms). The general structure of unbranched siloxanes is H3Si[OSiH2]nOSiH3. H3Si[OSiH2]nOSiH[OSiH2OSiH3]2 is an example of a branched siloxane. By extension hydrocarbyl derivatives are commonly included.

Not available