Compound Identification
SMILES
CC(=C)C(=O)OCCCC[Si](C)(O[Si](C)(C)C=C)O[Si](C)(C)C=C
InChIKey
InChIKey=JZLUMWZLBHXERD-UHFFFAOYSA-N
Formula
C17H34O4Si3
Mass
386.71
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organometallic compounds
-
Class
Organometalloid compounds
-
Subclass
Organosilicon compounds
- Level 5 Siloxanes
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Subclass
Organosilicon compounds
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Class
Organometalloid compounds
-
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
Enoate esters Organoheterosilanes Organic metalloid salts Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic acyclic compounds
Substituents
Siloxane - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Carboxylic acid ester - Organoheterosilane - Organic metalloid salt - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - 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