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Details

Stereochemistry MIXED
Molecular Formula C11H22O4Si
Molecular Weight 246.3755
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3,4-EPOXYCYCLOHEXYLETHYLTRIMETHOXYSILANE

SMILES

CO[Si](CCC1CCC2OC2C1)(OC)OC

InChI

InChIKey=DQZNLOXENNXVAD-UHFFFAOYSA-N
InChI=1S/C11H22O4Si/c1-12-16(13-2,14-3)7-6-9-4-5-10-11(8-9)15-10/h9-11H,4-8H2,1-3H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis of functionalized mesoporous material with various organo-silanes.
2010-01
Nitrite biosensing via selective enzymes--a long but promising route.
2010
Refractive index control and Rayleigh scattering properties of transparent TiO2 nanohybrid polymer.
2009-07-30
Amperometric biosensor for hydrogen peroxide based on coimmobilized horseradish peroxidase and methylene green in ormosils matrix with multiwalled carbon nanotubes.
2009-06-30
Size-controlled, one-pot synthesis, characterization, and biological applications of epoxy-organosilica particles possessing positive zeta potential.
2008-11-04
Application of lactate amperometric sol-gel biosensor to sequential injection determination of L-lactate.
2007-03-12
A conductive ormosil encapsulated with ferrocene conjugate and multiwall carbon nanotubes for biosensing application.
2006-03
Amperometric biosensor for hydrogen peroxide based on ferrocene-bovine serum albumin and multiwall carbon nanotube modified ormosil composite.
2006-02-15
Chiral speciation and determination of DL-selenomethionine enantiomers on a novel chiral ligand-exchange stationary phase.
2005-03
A new type of chemically bonded phase for reversed-phase HPLC.
2003-10
The copolymerization of carbon dioxide and [2-(3,4-epoxycyclohexyl)ethyl]trimethoxysilane catalyzed by (salen)CrCl. Formation of a CO2 soluble polycarbonate.
2003-07-28
[Preparation and evaluation of alkyl ether-bonded phase for reversed-phase high performance liquid chromatography].
2001-11
Patents

Patents

Name Type Language
3,4-EPOXYCYCLOHEXYLETHYLTRIMETHOXYSILANE
Systematic Name English
NSC-139838
Preferred Name English
BETA-(3,4-EPOXYCYCLOHEXYL)ETHYLTRIMETHOXYSILANE
Systematic Name English
SILANE, TRIMETHOXY(2-(7-OXABICYCLO(4.1.0)HEPT-3-YL)ETHYL)-
Systematic Name English
E 6250
Common Name English
(.BETA.-(3,4-EPOXYCYCLOHEXYL)ETHYL)TRIMETHOXYSILANE
Systematic Name English
(2-(3,4-EPOXYCYCLOHEXYL)ETHYL)TRIMETHOXYSILANE
Systematic Name English
7-OXABICYCLO(4.1.0)HEPTANE, 3-(2-(TRIMETHOXYSILYL)ETHYL)-
Systematic Name English
EPOXYCYCLOHEXYLETHYLTRIMETHOXYSILANE
Systematic Name English
3-(2-(TRIMETHOXYSILYL)ETHYL)-7-OXABICYCLO(4.1.0)HEPTANE
Systematic Name English
TRIMETHOXY(2-(7-OXABICYCLO(4.1.0)HEPT-3-YL)ETHYL)SILANE
Systematic Name English
4-(2-(TRIMETHOXYSILYL)ETHYL)-7-OXABICYCLO(4.1.0)HEPTANE
Systematic Name English
Code System Code Type Description
FDA UNII
SXJ79LS078
Created by admin on Mon Mar 31 21:57:30 GMT 2025 , Edited by admin on Mon Mar 31 21:57:30 GMT 2025
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EPA CompTox
DTXSID1043910
Created by admin on Mon Mar 31 21:57:30 GMT 2025 , Edited by admin on Mon Mar 31 21:57:30 GMT 2025
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PUBCHEM
18819
Created by admin on Mon Mar 31 21:57:30 GMT 2025 , Edited by admin on Mon Mar 31 21:57:30 GMT 2025
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CAS
3388-04-3
Created by admin on Mon Mar 31 21:57:30 GMT 2025 , Edited by admin on Mon Mar 31 21:57:30 GMT 2025
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NSC
139838
Created by admin on Mon Mar 31 21:57:30 GMT 2025 , Edited by admin on Mon Mar 31 21:57:30 GMT 2025
PRIMARY
SMS_ID
300000052937
Created by admin on Mon Mar 31 21:57:30 GMT 2025 , Edited by admin on Mon Mar 31 21:57:30 GMT 2025
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ECHA (EC/EINECS)
222-217-1
Created by admin on Mon Mar 31 21:57:30 GMT 2025 , Edited by admin on Mon Mar 31 21:57:30 GMT 2025
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