Compound Identification
SMILES
CCC(C)(SC(=S)N(C)C)C(=O)OCCC[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C
InChIKey
InChIKey=VFDBRYWCHSLQQI-UHFFFAOYSA-N
Formula
C18H41NO4S2Si3
Mass
483.9
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organometallic compounds
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Class
Organometalloid compounds
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Subclass
Organosilicon compounds
- Level 5 Siloxanes
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Subclass
Organosilicon compounds
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Class
Organometalloid compounds
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Superclass
Organometallic compounds
Kingdom
Organic compounds
Superclass
Organometallic compounds
Class
Organometalloid compounds
Subclass
Organosilicon compounds
Intermediate Tree Nodes
Not available
Direct Parent
Siloxanes
Alternative Parents
Fatty acid esters Trialkylheterosilanes Dithiocarbamic acid esters Carboxylic acid esters Sulfenyl compounds Organic metalloid salts Monocarboxylic acids and derivatives Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic acyclic compounds
Substituents
Siloxane - Fatty acid ester - Fatty acyl - Trialkylheterosilane - Dithiocarbamic acid ester - Carboxylic acid ester - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Sulfenyl compound - Organoheterosilane - Organic metalloid salt - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Organopnictogen compound - Organic nitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Aliphatic acyclic compound
Description
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.
External Descriptors
Not available