Catalog No.:AA003ETK

7589-27-7 | 4-Fluorophenethyl alcohol

Name: Name:4-Fluorophenethyl alcohol
Brand: AABLOCKS
SKU: AA003ETK
Availability: InStock
Rating: 90 (10 reviews)

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Quantity

98%

in stock

$13.00 $9.00

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10g

98%

in stock

$19.00 $14.00

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25g

98%

in stock

$43.00 $30.00

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100g

98%

in stock

$126.00 $89.00

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500g

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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature
Request for Quotation
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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA003ETK

Chemical Name:

4-Fluorophenethyl alcohol

CAS Number:

7589-27-7

Molecular Formula:

C8H9FO

Molecular Weight:

140.1549

MDL Number:

MFCD00002898

SMILES:

OCCc1ccc(cc1)F

Properties

BP:

213°C at 760 mmHg

Form:

Liquid

Refractive Index:

n20/D 1.507(lit.)

Storage:

Keep in dry area;Room Temperature;

Computed Properties

Complexity:

87.3

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

0.9

Upstream Synthesis Route

7589-27-7

459-31-4

[1]TetrahedronAsymmetry,2001,vol.12,#4,p.585-596

7589-27-7

332-42-3

[1]JournalofOrganicChemistry,2006,vol.71,#18,p.7035-7044

[2]TetrahedronAsymmetry,2001,vol.12,#4,p.585-596

[3]Patent:US2002/19531,2002,A1,

[4]BioorganicandMedicinalChemistry,2009,vol.17,#8,p.2989-3002

[5]Patent:EP2508526,2012,A1,.Locationinpatent:Page/Pagecolumn48

[6]Patent:WO2012/130915,2012,A1,.Locationinpatent:Page/Pagecolumn59

[7]BioorganicandMedicinalChemistryLetters,2001,vol.11,#4,p.495-500

[8]Patent:EP1734037,2006,A2,.Locationinpatent:Page/Pagecolumn70-71

[9]JournaloftheAmericanChemicalSociety,1941,vol.63,p.602,603

[10]HelveticaChimicaActa,1973,vol.56,p.2460-2479

[11]TetrahedronAsymmetry,1998,vol.9,#15,p.2725-2737

[12]HelveticaChimicaActa,2004,vol.87,#3,p.580-591

[13]BioorganicandMedicinalChemistryLetters,2006,vol.16,#18,p.4752-4756

[14]BioorganicandMedicinalChemistryLetters,2008,vol.18,#4,p.1515-1519

[15]Patent:WO2008/61688,2008,A1,.Locationinpatent:Page/Pagecolumn33

[16]JournalofMedicinalChemistry,2011,vol.54,#7,p.2282-2292

7589-27-7

497-19-8

332-42-3

[1]Patent:US5677324,1997,A,

7589-27-7

7789-60-8

332-42-3

[1]Patent:US2002/151717,2002,A1,

7589-27-7

1583-88-6

[1]JournaloftheAmericanChemicalSociety,1941,vol.63,p.602,603

Downstream Synthesis Route

7589-27-7

332-42-3

[1]JournalofOrganicChemistry,2006,vol.71,p.7035-7044

[2]TetrahedronAsymmetry,2001,vol.12,p.585-596

[3]Patent:US2002/19531,2002,A1

[4]BioorganicandMedicinalChemistry,2009,vol.17,p.2989-3002

[5]Patent:EP2508526,2012,A1.Locationinpatent:Page/Pagecolumn48

[6]Patent:WO2012/130915,2012,A1.Locationinpatent:Page/Pagecolumn59

[7]BioorganicandMedicinalChemistryLetters,2001,vol.11,p.495-500

[8]Patent:EP1734037,2006,A2.Locationinpatent:Page/Pagecolumn70-71

[9]JournaloftheAmericanChemicalSociety,1941,vol.63,p.602,603

[10]HelveticaChimicaActa,1973,vol.56,p.2460-2479

[11]TetrahedronAsymmetry,1998,vol.9,p.2725-2737

[12]HelveticaChimicaActa,2004,vol.87,p.580-591

[13]BioorganicandMedicinalChemistryLetters,2006,vol.16,p.4752-4756

[14]BioorganicandMedicinalChemistryLetters,2008,vol.18,p.1515-1519

[15]Patent:WO2008/61688,2008,A1.Locationinpatent:Page/Pagecolumn33

[16]JournalofMedicinalChemistry,2011,vol.54,p.2282-2292

[17]GreenChemistry,2019,vol.21,p.4324-4328

7589-27-7

332-43-4

[1]Baddeley;Bennett[JournaloftheChemicalSociety,1935,p.1819]

[2]Kitching,W.etal.[JournalofOrganometallicChemistry,1972,vol.42,p.373-390]

[3]CurrentPatentAssignee:MERCK&COINC-US2002/165241,2002,A1

[4]Cui,Hai-Bo;Xie,Ling-Zhi;Wan,Nan-Wei;He,Qing;Li,Zhi;Chen,Yong-Zheng[GreenChemistry,2019,vol.21,#16,p.4324-4328]

[5]CurrentPatentAssignee:MERCK&COINC-US2003/119811,2003,A1

7589-27-7

79-11-8

81228-04-8

[1]Locationinpatent:schemeortablePeters,Jens-Uwe;Kühne,Holger;Dehmlow,Henrietta;Grether,Uwe;Conte,Aurelia;Hainzl,Dominik;Hertel,Cornelia;Kratochwil,NicoleA.;Otteneder,Michael;Narquizian,Robert;Panousis,ConstantinosG.;Ricklin,Fabienne;Röver,Stephan[BioorganicandMedicinalChemistryLetters,2010,vol.20,#18,p.5426-5430]

[2]CurrentPatentAssignee:UNIVERSITYOFNOTTINGHAM-WO2012/4549,2012,A1Locationinpatent:Page/Pagecolumn20

[3]Mistry,ShaileshN.;Baker,JillianG.;Fischer,PeterM.;Hill,StephenJ.;Gardiner,SheilaM.;Kellam,Barrie[JournalofMedicinalChemistry,2013,vol.56,#10,p.3852-3865]

[4]Machin,PeterJ.;Hurst,DavidN.;Bradshaw,RachelM.;Blaber,LeslieC.;Burden,DavidT.;etal.[JournalofMedicinalChemistry,1983,vol.26,#11,p.1570-1576]

7589-27-7

124-63-0

40759-47-5

[1]CurrentPatentAssignee:CHRYSALISINVESTMENTSLIMITED-WO2017/143011,2017,A1Locationinpatent:Paragraph0434-0436

[2]Patrick,GrahamL.[JournaloftheChemicalSociety.PerkintransactionsI,1995,#10,p.1273-1280]

[3]CurrentPatentAssignee:SANOFI-US2002/151717,2002,A1

[4]CurrentPatentAssignee:SANOFI-US2005/261341,2005,A1

[5]CurrentPatentAssignee:SANOFI-EP1734037,2006,A2Locationinpatent:Page/Pagecolumn26

[6]CurrentPatentAssignee:DAEWOONGPHARMACEUTICALCO.,LTD.;KOREARESEARCHINSTITUTEOFCHEMICALTECHNOLOGY-WO2008/16278,2008,A1Locationinpatent:Page/Pagecolumn8-9

[7]Liu,Jing-Hui;Yang,Chu-Ting;Lu,Xiao-Yu;Zhang,Zhen-Qi;Xu,Ling;Cui,Mian;Lu,Xi;Xiao,Bin;Fu,Yao;Liu,Lei[Chemistry-AEuropeanJournal,2014,vol.20,#47,p.15334-15338]

Literature

Title: Chiral recognition between 1-(4-fluorophenyl)ethanol and 2-butanol: higher binding energy of homochiral complexes in the gas phase.

Journal: Physical chemistry chemical physics : PCCP 20110121

Title: Water binding sites in 2-para- and 2-ortho-fluorophenylethanol: a high-resolution UV experiment and ab initio calculations.

Journal: The Journal of chemical physics 20101121

Title: Mass analysed threshold ionisation spectroscopy of flexible 2-para-fluorophenylethanol conformers with and without an intramolecular OH...pi bond.

Journal: Physical chemistry chemical physics : PCCP 20090407

Title: Fluorine substitution and nonconventional OH...pi intramolecular bond: high-resolution UV spectroscopy and ab initio calculations of 2-(p-fluorophenyl)ethanol.

Journal: Physical chemistry chemical physics : PCCP 20080521

Title: Synthesis and application of mono-6-(3-methylimidazolium)-6-deoxyperphenylcarbamoyl-beta-cyclodextrin chloride as chiral stationary phases for high-performance liquid chromatography and supercritical fluid chromatography.

Journal: Journal of chromatography. A 20080222

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