IMPPAT Phytochemical information: 
3-Isopropoxy-1,1,1,7,7,7-hexamethyl-3,5,5-tris(trimethylsiloxy)tetrasiloxane

3-Isopropoxy-1,1,1,7,7,7-hexamethyl-3,5,5-tris(trimethylsiloxy)tetrasiloxane
Summary

IMPPAT Phytochemical identifier: IMPHY016368

Phytochemical name: 3-Isopropoxy-1,1,1,7,7,7-hexamethyl-3,5,5-tris(trimethylsiloxy)tetrasiloxane

Synonymous chemical names:
3-isopropoxy-1,1,1,7,7,7-hexamethyl-3,5,5-tris(trimethylsiloxy)tetrasiloxane

External chemical identifiers:
CID:553025, ChEBI:144334
Chemical structure information

SMILES:
CC(O[Si](O[Si](O[Si](C)(C)C)(O[Si](C)(C)C)O[Si](C)(C)C)(O[Si](C)(C)C)O[Si](C)(C)C)C

InChI:
InChI=1S/C18H52O7Si7/c1-18(2)19-31(20-26(3,4)5,21-27(6,7)8)25-32(22-28(9,10)11,23-29(12,13)14)24-30(15,16)17/h18H,1-17H3

InChIKey:
MODCFEJKGWZWCR-UHFFFAOYSA-N

DeepSMILES:
CCO[Si]O[Si]O[Si]C)C)C)))O[Si]C)C)C)))O[Si]C)C)C)))))O[Si]C)C)C)))O[Si]C)C)C)))))C

Functional groups:
CO[Si](O[Si](C)(C)C)(O[Si](C)(C)C)O[Si](O[Si](C)(C)C)(O[Si](C)(C)C)O[Si](C)(C)C
Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass:
Organometallic compounds

ClassyFire Class: Organometalloid compounds

ClassyFire Subclass: Organosilicon compounds

NP Classifier Biosynthetic pathway: Alkaloids

NP Classifier Superclass: Tyrosine alkaloids

NP Classifier Class: Phenylethylamines

NP-Likeness score: -0.034


Chemical structure download