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

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 CYCLOPENTANOL

SMILES

OC1CCCC1

InChI

InChIKey=XCIXKGXIYUWCLL-UHFFFAOYSA-N
InChI=1S/C5H10O/c6-5-3-1-2-4-5/h5-6H,1-4H2

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Phthalazine PDE4 inhibitors. Part 2: the synthesis and biological evaluation of 6-methoxy-1,4-disubstituted derivatives.
2001 Jan 8
Methanobacterium congolense sp. nov., from a methanogenic fermentation of cassava peel.
2001 Mar
An experimental and computational study of 1,2-hydrogen migrations in 2-hydroxycyclopentylidene and its conjugate base.
2001 Mar 9
Improving metabolic stability of phosphodiesterase-4 inhibitors containing a substituted catechol: prevention of reactive intermediate formation and covalent binding.
2002 Aug 19
Phthalazine PDE4 inhibitors. Part 3: the synthesis and in vitro evaluation of derivatives with a hydrogen bond acceptor.
2002 Jan 7
Effects of topical mydriatics and vasoconstrictors on prostaglandin-E2-induced aqueous flare elevation in pigmented rabbits.
2003 Sep-Oct
Thermodynamics of the molecular and chiral recognition of cycloalkanols and camphor by modified beta-cyclodextrins possessing simple aromatic tethers.
2004 Jan 9
Detector for liquid chromatography based on acoustic emissions from an oscillating flame.
2004 Sep 15
High-pressure polymorphism of cyclopentanol (C5H10O): the structure of cyclopentanol phase-V at 1.5 GPa.
2005 Sep
Evaluation of PDE4 inhibition for COPD.
2006
Chiral microemulsion electrokinetic chromatography: Effect of cosurfactant identity on enantioselectivity, methylene selectivity, resolution, and other chromatographic figures of merit.
2006 Nov
Analysis of volatile compounds as spoilage indicators in fresh king salmon (Oncorhynchus tshawytscha) during storage using SPME-GC-MS.
2006 Nov 1
Stereoselective preparation of a cyclopentane-based NK1 receptor antagonist bearing an unsymmetrically substituted sec-sec ether.
2006 Sep 15
Diastereoselective multicomponent cyclizations of Fischer carbene complexes, lithium enolates, and allylmagnesium bromide leading to highly substituted five- and six-membered carbocycles.
2006 Sep 18
The changes of posterior corneal surface and high-order aberrations after refractive surgery in moderate myopia.
2007 Sep
Search for a correlation between telomere length and severity of retinitis pigmentosa due to the dominant rhodopsin Pro23His mutation.
2009
Nummular keratopathy in a patient with Hyper-IgD Syndrome.
2009 Aug 5
The effect of epiblepharon surgery on visual acuity and with-the-rule astigmatism in children.
2010 Dec
Use of visual acuity to screen for significant refractive errors in adolescents: is it reliable?
2010 Jul
Three-component coupling reactions of silyl glyoxylates, vinyl Grignard reagent, and nitroalkenes: an efficient, highly diastereoselective approach to nitrocyclopentanols.
2010 Nov 15
Tumor necrosis factor and its receptors in the neuroretina and retinal vasculature after ischemia-reperfusion injury in the pig retina.
2010 Nov 6
Changes in protein profiles of guinea pig sclera during development of form deprivation myopia and recovery.
2010 Oct 27
Patents
Name Type Language
CYCLOPENTANOL
MI  
Systematic Name English
UN-2244
Code English
HYDROXYCYCLOPENTANE
Systematic Name English
NSC-49117
Code English
1-CYCLOPENTANOL
Systematic Name English
UN2244
Code English
CYCLOPENTYL ALCOHOL
Systematic Name English
CYCLOPENTANOL [MI]
Common Name English
Code System Code Type Description
MESH
C016327
Created by admin on Sat Dec 16 02:16:46 GMT 2023 , Edited by admin on Sat Dec 16 02:16:46 GMT 2023
PRIMARY
WIKIPEDIA
CYCLOPENTANOL
Created by admin on Sat Dec 16 02:16:46 GMT 2023 , Edited by admin on Sat Dec 16 02:16:46 GMT 2023
PRIMARY
CHEBI
16133
Created by admin on Sat Dec 16 02:16:46 GMT 2023 , Edited by admin on Sat Dec 16 02:16:46 GMT 2023
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EPA CompTox
DTXSID1033371
Created by admin on Sat Dec 16 02:16:46 GMT 2023 , Edited by admin on Sat Dec 16 02:16:46 GMT 2023
PRIMARY
ECHA (EC/EINECS)
202-504-8
Created by admin on Sat Dec 16 02:16:46 GMT 2023 , Edited by admin on Sat Dec 16 02:16:46 GMT 2023
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HSDB
2821
Created by admin on Sat Dec 16 02:16:46 GMT 2023 , Edited by admin on Sat Dec 16 02:16:46 GMT 2023
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PUBCHEM
7298
Created by admin on Sat Dec 16 02:16:46 GMT 2023 , Edited by admin on Sat Dec 16 02:16:46 GMT 2023
PRIMARY
MERCK INDEX
m4007
Created by admin on Sat Dec 16 02:16:46 GMT 2023 , Edited by admin on Sat Dec 16 02:16:46 GMT 2023
PRIMARY Merck Index
FDA UNII
1L43Q07TBU
Created by admin on Sat Dec 16 02:16:46 GMT 2023 , Edited by admin on Sat Dec 16 02:16:46 GMT 2023
PRIMARY
CAS
96-41-3
Created by admin on Sat Dec 16 02:16:46 GMT 2023 , Edited by admin on Sat Dec 16 02:16:46 GMT 2023
PRIMARY
NSC
49117
Created by admin on Sat Dec 16 02:16:46 GMT 2023 , Edited by admin on Sat Dec 16 02:16:46 GMT 2023
PRIMARY