Compound Identification
SMILES
CCCC[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)CC(C)OCCOC(=O)C(C)=C
InChIKey
InChIKey=IFKUNYFVGJMTTB-UHFFFAOYSA-N
Formula
C23H54O7Si5
Mass
583.103
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organometallic compounds
-
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
-
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
Trialkylheterosilanes Enoate esters Organic metalloid salts Monocarboxylic acids and derivatives Dialkyl ethers Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic acyclic compounds
Substituents
Siloxane - Trialkylheterosilane - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Carboxylic acid ester - Carboxylic acid derivative - Dialkyl ether - Ether - Monocarboxylic acid or derivatives - Organoheterosilane - Organic metalloid salt - Organic oxygen compound - Organooxygen compound - Carbonyl group - Organic oxide - Hydrocarbon derivative - 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