Compound Identification
SMILES
[Y].[Y].[Y].CC(=C)C(=O)OCCC[Si](C)(O)O[Si](C)(C)O[Al](O[Si](C)(C)O)O[Si](C)(C)O
InChIKey
InChIKey=SCAAYOJDOZVQGO-UHFFFAOYSA-N
Formula
C14H35AlO9Si4Y3
Mass
753.464
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
Enoate esters Silanols Organoheterosilanes Organic transition metal salts Organic metalloid salts Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic acyclic compounds
Substituents
Siloxane - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Carboxylic acid ester - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Silanol - Organoheterosilane - Organic transition metal salt - Organic metalloid salt - Organic metal salt - Organic oxygen compound - Organic oxide - Carbonyl group - Organooxygen compound - 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