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Details

Stereochemistry ACHIRAL
Molecular Formula C6H6O
Molecular Weight 94.1112
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FURAN, 2-ETHENYL-

SMILES

C=CC1=CC=CO1

InChI

InChIKey=QQBUHYQVKJQAOB-UHFFFAOYSA-N
InChI=1S/C6H6O/c1-2-6-4-3-5-7-6/h2-5H,1H2

HIDE SMILES / InChI

Molecular Formula C6H6O
Molecular Weight 94.1112
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
The ERAD inhibitor Eeyarestatin I is a bifunctional compound with a membrane-binding domain and a p97/VCP inhibitory group.
2010-11-12
Formation enthalpies and bond dissociation energies of alkylfurans. The strongest CX bonds known?
2009-04-30
Complete 1H and 13C NMR assignment of trans,trans-2,3-divinylfuran derivatives.
2007-08
In vivo genotoxic evaluation of the furylethylene derivative 1-(5-bromofur-2-yl)-2-nitroethene in mouse bone marrow.
2005-07
Comparative genotoxic evaluation of 2-furylethylenes and 5-nitrofurans by using the comet assay in TK6 cells.
2005-05
Atom, atom-type and total molecular linear indices as a promising approach for bioorganic and medicinal chemistry: theoretical and experimental assessment of a novel method for virtual screening and rational design of new lead anthelmintic.
2005-02-15
Total and local (atom and atom type) molecular quadratic indices: significance interpretation, comparison to other molecular descriptors, and QSPR/QSAR applications.
2004-12-15
On the valence shell electronic spectroscopy of 2-vinyl furan.
2004-06-15
Synthesis, topoisomerase I inhibition and structure-activity relationship study of 2,4,6-trisubstituted pyridine derivatives.
2004-03-08
Genotoxicity testing of the furylethylene derivative 1-(5-bromofur-2-yl)-2-bromo-2-nitroethene in cultured human lymphocytes.
2004-02
In vitro genotoxicity testing of the furylethylene derivative UC-245 in human cells.
2004-01
Micronuclei to detect in vivo chemotherapy damage in a p53 mutated solid tumour.
2003-08-18
The mutagenic potential of the furylethylene derivative 2-furyl-1-nitroethene in the mouse bone marrow micronucleus test.
2003-04
Genotoxic evaluation of the furylethylene derivative 1-(5-bromofur-2-yl)-2-nitroethene in cultured human lymphocytes.
2002-08-26
Genotoxic evaluation of the furylethylene derivative 2-furyl-1-nitroethene in cultured human lymphocytes.
2001-10-18
3D connectivity indices in QSPR/QSAR studies.
2001-06-21
Synthesis of D- and L-deoxymannojirimycin via an asymmetric aminohydroxylation of vinylfuran.
2001-02-08
Novel local (fragment-based) topological molecular descriptors for QSpr/QSAR and molecular design.
2001
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:50:48 GMT 2025
Edited
by admin
on Mon Mar 31 19:50:48 GMT 2025
Record UNII
V5MN67I54D
Record Status Validated (UNII)
Record Version
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Name Type Language
2-ETHENYLFURAN
Preferred Name English
FURAN, 2-ETHENYL-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID8073261
Created by admin on Mon Mar 31 19:50:48 GMT 2025 , Edited by admin on Mon Mar 31 19:50:48 GMT 2025
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PUBCHEM
73881
Created by admin on Mon Mar 31 19:50:48 GMT 2025 , Edited by admin on Mon Mar 31 19:50:48 GMT 2025
PRIMARY
FDA UNII
V5MN67I54D
Created by admin on Mon Mar 31 19:50:48 GMT 2025 , Edited by admin on Mon Mar 31 19:50:48 GMT 2025
PRIMARY
CAS
1487-18-9
Created by admin on Mon Mar 31 19:50:48 GMT 2025 , Edited by admin on Mon Mar 31 19:50:48 GMT 2025
PRIMARY