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Details

Stereochemistry ACHIRAL
Molecular Formula C5H10O
Molecular Weight 86.1323
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-PENTENOL

SMILES

OCCCC=C

InChI

InChIKey=LQAVWYMTUMSFBE-UHFFFAOYSA-N
InChI=1S/C5H10O/c1-2-3-4-5-6/h2,6H,1,3-5H2

HIDE SMILES / InChI

Molecular Formula C5H10O
Molecular Weight 86.1323
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Strictosidine activation in Apocynaceae: towards a "nuclear time bomb"?
2010-08-19
Characterization of 1-hydroxy-2-methyl-2-(E)-butenyl-4-diphosphate synthase (HDS) gene from Ginkgo biloba.
2010-02
Comparative transcripts profiling reveals new insight into molecular processes regulating lycopene accumulation in a sweet orange (Citrus sinensis) red-flesh mutant.
2009-11-18
Optimization of the transient transformation of Catharanthus roseus cells by particle bombardment and its application to the subcellular localization of hydroxymethylbutenyl 4-diphosphate synthase and geraniol 10-hydroxylase.
2009-08
Isomer-specific influences on the composition of reaction intermediates in dimethyl ether/propene and ethanol/propene flame.
2008-10-02
Contribution of hydroxymethylbutenyl diphosphate synthase to carotenoid biosynthesis in bacteria and plants.
2008-07-04
Highly efficient asymmetric synthesis of fluvirucinine A1 via Zr-catalyzed asymmetric carboalumination of alkenes (ZACA)-lipase-catalyzed acetylation tandem process.
2008-01-17
Spatial distribution and hormonal regulation of gene products from methyl erythritol phosphate and monoterpene-secoiridoid pathways in Catharanthus roseus.
2007-09
Possible direct involvement of the active-site [4Fe-4S] cluster of the GcpE enzyme from Thermus thermophilus in the conversion of MEcPP.
2007-01-23
Characterizing ionic liquids as reaction media through a chemical probe.
2007
On the stereoselectivity of 4-penten-1-oxyl radical 5-exo-trig cyclizations.
2006-11-21
Asymmetric synthesis of anti-1,2-amino alcohols via the Borono-Mannich reaction: a formal synthesis of (-)-swainsonine.
2006-09-01
Precise investigation of the axial ligand substitution mechanism on a hydrogenphosphato-bridged lantern-type platinum(III) binuclear complex in acidic aqueous solution.
2005-10-31
The Arabidopsis csb3 mutant reveals a regulatory link between salicylic acid-mediated disease resistance and the methyl-erythritol 4-phosphate pathway.
2005-10
Cyanobacterial non-mevalonate pathway: (E)-4-hydroxy-3-methylbut-2-enyl diphosphate synthase interacts with ferredoxin in Thermosynechococcus elongatus BP-1.
2005-05-27
Synthesis of unsaturated amino alcohols through unexpectedly selective Ru-catalyzed cross-metathesis reactions.
2005-05-26
Alpha-N-acetylmannosamine (ManNAc) synthesis via rhodium(II)-catalyzed oxidative cyclization of glucal 3-carbamates.
2005-05-13
On the 6-endo selectivity in 4-penten-1-oxyl radical cyclizations.
2004-09-29
Mechanism of the axial ligand substitution reactions on the head-to-tail alpha-pyridonato-bridged cis-diammineplatinum(III) dinuclear complex with olefins.
2004-01-12
Glycosynthase-catalysed syntheses at pH below neutrality.
2003-11-17
A genetic basis for human gammadelta T-cell reactivity towards microbial pathogens.
2003-08
Bioinformatic and molecular analysis of hydroxymethylbutenyl diphosphate synthase (GCPE) gene expression during carotenoid accumulation in ripening tomato fruit.
2003-07
Mechanism of ketone and alcohol formations from alkenes and alkynes on the head-to-head 2-pyridonato-bridged cis-diammineplatinum(III) dinuclear complex.
2003-03-26
Functional characterization of GcpE, an essential enzyme of the non-mevalonate pathway of isoprenoid biosynthesis.
2002-12-18
Isoprenoid biosynthesis through the methylerythritol phosphate pathway: the (E)-4-hydroxy-3-methylbut-2-enyl diphosphate synthase (GcpE) is a [4Fe-4S] protein.
2002-11-15
Biosynthesis of terpenes. Preparation of (E)-1-hydroxy-2-methyl-but-2-enyl 4-diphosphate, an intermediate of the deoxyxylulose phosphate pathway.
2002-06-28
Identification of (E)-4-hydroxy-3-methyl-but-2-enyl pyrophosphate as a major activator for human gammadelta T cells in Escherichia coli.
2001-12-07
Cutting edge: human gamma delta T cells are activated by intermediates of the 2-C-methyl-D-erythritol 4-phosphate pathway of isoprenoid biosynthesis.
2001-03-15
Identification of gcpE as a novel gene of the 2-C-methyl-D-erythritol 4-phosphate pathway for isoprenoid biosynthesis in Escherichia coli.
2001-01-19
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:40:02 GMT 2025
Edited
by admin
on Mon Mar 31 22:40:02 GMT 2025
Record UNII
W0558TQC6F
Record Status Validated (UNII)
Record Version
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Name Type Language
4-PENTENOL
Systematic Name English
1-HYDROXY-4-PENTENE
Preferred Name English
5-HYDROXY-1-PENTENE-
Systematic Name English
4-PENTENYL ALCOHOL
Systematic Name English
NSC-97503
Code English
1-PENTEN-5-OL
Systematic Name English
4-PENTEN-1-OL
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID30231562
Created by admin on Mon Mar 31 22:40:02 GMT 2025 , Edited by admin on Mon Mar 31 22:40:02 GMT 2025
PRIMARY
CAS
821-09-0
Created by admin on Mon Mar 31 22:40:02 GMT 2025 , Edited by admin on Mon Mar 31 22:40:02 GMT 2025
PRIMARY
PUBCHEM
13181
Created by admin on Mon Mar 31 22:40:02 GMT 2025 , Edited by admin on Mon Mar 31 22:40:02 GMT 2025
PRIMARY
FDA UNII
W0558TQC6F
Created by admin on Mon Mar 31 22:40:02 GMT 2025 , Edited by admin on Mon Mar 31 22:40:02 GMT 2025
PRIMARY
ECHA (EC/EINECS)
212-473-2
Created by admin on Mon Mar 31 22:40:02 GMT 2025 , Edited by admin on Mon Mar 31 22:40:02 GMT 2025
PRIMARY
NSC
97503
Created by admin on Mon Mar 31 22:40:02 GMT 2025 , Edited by admin on Mon Mar 31 22:40:02 GMT 2025
PRIMARY