U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C9H10O
Molecular Weight 134.1751
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-VINYLANISOLE

SMILES

COC1=CC=C(C=C)C=C1

InChI

InChIKey=UAJRSHJHFRVGMG-UHFFFAOYSA-N
InChI=1S/C9H10O/c1-3-8-4-6-9(10-2)7-5-8/h3-7H,1H2,2H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Kinetic isotope effects in cycloreversion of rhenium (V) diolates.
2002 Apr 17
Catalytic hydrophosphination of styrenes.
2002 Mar 7
Substituent effects on the ionization reaction of beta-mesylate phenethyl radicals.
2003 Jun 7
Steam distillation-solid-phase microextraction for the detection of Ephedra sinica in herbal preparations.
2004 Jan 30
Generation and absolute reactivity of an aryl enol radical cation in solution.
2004 Jul 23
The electron-poor phosphines P{C6H3(CF3)2-3,5}3 and P(C6F5)3 do not mimic phosphites as ligands for hydroformylation. A comparison of the coordination chemistry of P{C6H3(CF3)2-3,5}3 and P(C6F5)3 and the unexpectedly low hydroformylation activity of their rhodium complexes.
2005 Apr 7
High molar mass polymers by cationic polymerisation in emulsion and miniemulsion.
2005 Jun 7
Synthesis of functionalized asymmetric star polymers containing conductive polyacetylene segments by living anionic polymerization.
2005 Oct 19
Synthesis, characterization and olefin/CO exchange reactions of pyrazolylborato complexes of copper(I).
2006 Aug 7
Acyclic or long-bond intermediate in the electron-transfer-catalyzed dimerization of 4-methoxystyrene.
2006 Nov 10
A simple technique to grow polymer brushes using in situ surface ligation of an organometallic initiator.
2006 Oct 11
Revealing shape selectivity and catalytic activity trends within the pores of H-ZSM-5 crystals by time- and space-resolved optical and fluorescence microspectroscopy.
2007
Visualizing the crystal structure and locating the catalytic activity of micro- and mesoporous ZSM-5 zeolite crystals by using in situ optical and fluorescence microscopy.
2008
Selectivity in the electron transfer catalyzed Diels-Alder reaction of (R)-alpha-phellandrene and 4-methoxystyrene.
2008 Oct 17
N,N'-(Biphenyl-2,2'-di-yl)bis-(furan-2-carboxamide).
2009 Jun 13
Short-step synthesis of a resveratrol derivative from commercially available 1,3-dimethoxybenzene and 4-vinylanisole.
2009 Nov
Formal [4 + 2] cycloaddition of donor-acceptor cyclobutanes and aldehydes: stereoselective access to substituted tetrahydropyrans.
2009 Oct 14
A mechanistic investigation on copolymerization of ethylene with polar monomers using a cyclophane-based Pd(II) alpha-diimine catalyst.
2009 Sep 2
Cationic polymerization of vinyl monomers in aqueous media: from monofunctional oligomers to long-lived polymer chains.
2010 Mar 16
Patents
Name Type Language
4-VINYLANISOLE
Systematic Name English
NSC-408326
Code English
NSC-42171
Code English
Code System Code Type Description
EPA CompTox
DTXSID7073222
Created by admin on Fri Dec 15 18:07:56 GMT 2023 , Edited by admin on Fri Dec 15 18:07:56 GMT 2023
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MESH
C534356
Created by admin on Fri Dec 15 18:07:56 GMT 2023 , Edited by admin on Fri Dec 15 18:07:56 GMT 2023
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CAS
637-69-4
Created by admin on Fri Dec 15 18:07:56 GMT 2023 , Edited by admin on Fri Dec 15 18:07:56 GMT 2023
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NSC
408326
Created by admin on Fri Dec 15 18:07:56 GMT 2023 , Edited by admin on Fri Dec 15 18:07:56 GMT 2023
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PUBCHEM
12507
Created by admin on Fri Dec 15 18:07:56 GMT 2023 , Edited by admin on Fri Dec 15 18:07:56 GMT 2023
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ECHA (EC/EINECS)
211-298-9
Created by admin on Fri Dec 15 18:07:56 GMT 2023 , Edited by admin on Fri Dec 15 18:07:56 GMT 2023
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NSC
42171
Created by admin on Fri Dec 15 18:07:56 GMT 2023 , Edited by admin on Fri Dec 15 18:07:56 GMT 2023
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FDA UNII
2ISH8T4A6E
Created by admin on Fri Dec 15 18:07:56 GMT 2023 , Edited by admin on Fri Dec 15 18:07:56 GMT 2023
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WIKIPEDIA
4-Vinylanisole
Created by admin on Fri Dec 15 18:07:56 GMT 2023 , Edited by admin on Fri Dec 15 18:07:56 GMT 2023
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