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Details

Stereochemistry ACHIRAL
Molecular Formula C6H12O
Molecular Weight 100.1589
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VINYL BUTYL ETHER

SMILES

CCCCOC=C

InChI

InChIKey=UZKWTJUDCOPSNM-UHFFFAOYSA-N
InChI=1S/C6H12O/c1-3-5-6-7-4-2/h4H,2-3,5-6H2,1H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Characterization of plasma polymerized C, H, and O containing compounds by MALDI mass spectrometry.
2010-11-16
2,6-Disubstituted and 2,2,6-trisubstituted piperidines from serine: asymmetric synthesis and further elaboration.
2010-08-06
A short stereoselective synthesis of racemic 2-epicalvine.
2010-08
Ligandless, anionic, arylpalladium halide intermediates in the Heck reaction.
2010-01-13
A novel method for the preparation of retinoic acid-loaded nanoparticles.
2009-05-19
Microflow system controlled carbocationic polymerization of vinyl ethers.
2008-09-01
Bioactive polymeric materials for targeted administration of active agents: synthesis and evaluation.
2008-06-11
A new biocompatible nanoparticle delivery system for the release of fibrinolytic drugs.
2008-06-05
Ruthenium-based olefin metathesis catalysts coordinated with unsymmetrical N-heterocyclic carbene ligands: synthesis, structure, and catalytic activity.
2008
Novel chlorhexidine releasing system developed from thermosensitive vinyl ether-based hydrogels.
2007-11
Novel in situ polymerized coatings for hydrophobic interaction chromatography media.
2007-08-17
Pd-mBDPP-catalyzed regioselective internal arylation of electron-rich olefins by aryl halides.
2006-09-15
Synthesis of pyrrolidines via palladium(II)-catalyzed aerobic oxidative carboamination of butyl vinyl ether and styrenes with allyl tosylamides.
2006-07-20
Kinetic study of the gas-phase reactions of OH and NO3 radicals and O3 with selected vinyl ethers.
2006-06-15
A hetero-Diels-Alder approach to complex pyrones: an improved synthesis of the spongistatin AB spiroketal.
2006-03-02
Iridium complex-catalyzed [2+2+2] cycloaddition of alpha,omega-diynes with monoynes and monoenes.
2006-01-20
Release kinetics of bovine serum albumin from pH-sensitive poly(vinyl ether) based hydrogels.
2005-01-20
Zirconium-mediated cross-coupling of terminal alkynes and vinyl bromides: selective synthesis of cyclobutene and 1,3-diene derivatives.
2004-01-05
Synthesis of allyl and alkyl vinyl ethers using an in situ prepared air-stable palladium catalyst. Efficient transfer vinylation of primary, secondary, and tertiary alcohols.
2003-06-27
Uses of thermoresponsive and RGD/insulin-modified poly(vinyl ether)-based hydrogels in cell cultures.
2003
Copper(I)-homoscorpionate catalysts for the preferential, kinetically controlled cis cyclopropanation of alpha-olefins with ethyl diazoacetate.
2002-02-13
Effect of fluorinated groups on photooxidative stability of polymeric protectives applied on marble.
2002-02-12
Palladium(II)-catalyzed transfer vinylation of protected monosaccharides.
2002-02-07
Palladium-catalyzed regioselective arylation of an electron-rich olefin by aryl halides in ionic liquids.
2001-01-25
Patents
Name Type Language
VINYL BUTYL ETHER
Systematic Name English
BUTYL VINYL ETHER
HSDB  
Preferred Name English
BUTANE, 1-(ETHENYLOXY)-
Systematic Name English
1-BUTOXYETHENE
Systematic Name English
VINIPOL VB 2
Common Name English
SHOSTAKOVSKI BALSAM
Common Name English
BUTYL VINYL ETHER [HSDB]
Common Name English
NSC-8264
Code English
ETHER, BUTYL VINYL
Systematic Name English
VINIPOL
Common Name English
1-(VINYLOXY)BUTANE
Systematic Name English
1-(ETHENYLOXY)BUTANE
Systematic Name English
N-BUTYL VINYL ETHER
Common Name English
BUTOXYETHENE
Systematic Name English
VINILIN
Common Name English
BUTYL VINYL ETHER, INHIBITED
Common Name English
VINYL N-BUTYL ETHER
Common Name English
Polyvinox [WHO-DD]
Common Name English
Code System Code Type Description
PUBCHEM
8108
Created by admin on Mon Mar 31 19:54:12 GMT 2025 , Edited by admin on Mon Mar 31 19:54:12 GMT 2025
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HSDB
6384
Created by admin on Mon Mar 31 19:54:12 GMT 2025 , Edited by admin on Mon Mar 31 19:54:12 GMT 2025
PRIMARY
EPA CompTox
DTXSID5051575
Created by admin on Mon Mar 31 19:54:12 GMT 2025 , Edited by admin on Mon Mar 31 19:54:12 GMT 2025
PRIMARY
MESH
C096129
Created by admin on Mon Mar 31 19:54:12 GMT 2025 , Edited by admin on Mon Mar 31 19:54:12 GMT 2025
PRIMARY
FDA UNII
321YRT7173
Created by admin on Mon Mar 31 19:54:12 GMT 2025 , Edited by admin on Mon Mar 31 19:54:12 GMT 2025
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NSC
8264
Created by admin on Mon Mar 31 19:54:12 GMT 2025 , Edited by admin on Mon Mar 31 19:54:12 GMT 2025
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CAS
111-34-2
Created by admin on Mon Mar 31 19:54:12 GMT 2025 , Edited by admin on Mon Mar 31 19:54:12 GMT 2025
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ECHA (EC/EINECS)
203-860-7
Created by admin on Mon Mar 31 19:54:12 GMT 2025 , Edited by admin on Mon Mar 31 19:54:12 GMT 2025
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SMS_ID
100000176404
Created by admin on Mon Mar 31 19:54:12 GMT 2025 , Edited by admin on Mon Mar 31 19:54:12 GMT 2025
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