Home Boronic Acids 214360-58-4
214360-58-4,MFCD03453665
Catalog No.:AA0038TD

214360-58-4 | 4-Fluorophenylboronic acid, pinacol ester

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1g
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in stock  
$6.00   $4.00
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5g
97%
in stock  
$13.00   $9.00
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10g
97%
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$15.00   $10.00
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25g
97%
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA0038TD
Chemical Name:
4-Fluorophenylboronic acid, pinacol ester
CAS Number:
214360-58-4
Molecular Formula:
C12H16BFO2
Molecular Weight:
222.0636
MDL Number:
MFCD03453665
SMILES:
CC1(C)OB(OC1(C)C)c1ccc(cc1)F
Properties
Computed Properties
 
Complexity:
244  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
3  
Rotatable Bond Count:
1  

Upstream Synthesis Route

[1]GreenChemistry,2015,vol.17,#6,p.3540-3551

[2]OrganicLetters,2014,vol.16,#7,p.1836-1839

[1]Patent:JP5966165,2016,B2,.Locationinpatent:Paragraph0056-0062

[2]JournaloftheAmericanChemicalSociety,2016,vol.138,#9,p.2985-2988

[3]AdvancedSynthesisandCatalysis,2016,vol.358,#6,p.977-983

[4]JournalofFluorineChemistry,2015,vol.178,p.195-201

[5]ACSCatalysis,2018,vol.8,#5,p.4049-4054

[6]JournaloftheAmericanChemicalSociety,2017,vol.139,#2,p.607-610

[7]Patent:WO2011/149950,2011,A2,.Locationinpatent:Page/Pagecolumn136-137

[8]OrganicandBiomolecularChemistry,2015,vol.13,#11,p.3236-3242

[9]JournalofOrganicChemistry,2015,vol.80,#19,p.9671-9681

[10]EuropeanJournalofInorganicChemistry,2015,vol.2015,#31,p.5226-5231

[11]BioorganicandMedicinalChemistryLetters,2018,vol.28,#14,p.2513-2517

[1]TetrahedronLetters,2016,vol.57,#14,p.1551-1554

[2]JournalofOrganicChemistry,2013,vol.78,#5,p.1923-1933

[3]TetrahedronLetters,2017,vol.58,#40,p.3851-3853

[4]AngewandteChemie-InternationalEdition,2010,vol.49,#10,p.1846-1849

[5]AngewandteChemie-InternationalEdition,2010,vol.49,#10,p.1846-1849

[6]Synlett,2014,vol.25,#11,p.1577-1584

[1]Synthesis(Germany),2017,vol.49,#21,p.4759-4768

[2]JournaloftheAmericanChemicalSociety,2017,vol.139,#2,p.607-610

[3]ChemicalScience,2016,vol.7,#6,p.3676-3680

[4]CatalysisCommunications,2016,vol.85,p.61-65

[1]JournaloftheAmericanChemicalSociety,2017,vol.139,#2,p.975-984

[2]Patent:KR2018/12458,2018,A,.Locationinpatent:Paragraph0049;0050;0055

Downstream Synthesis Route
380500-13-0    214360-58-4   
C20H17FN2 

[1]Pastine,StefanJ.;Gribkov,DenisV.;Sames,Dalibor[JournaloftheAmericanChemicalSociety,2006,vol.128,#44,p.14220-14221]

[1]Murray,PhilipR.D.;Browne,DuncanL.;Pastre,JulioC.;Butters,Chris;Guthrie,Duncan;Ley,StevenV.[OrganicProcessResearchandDevelopment,2013,vol.17,#9,p.1192-1208]

[2]Dienes,Yvonne;Durben,Stefan;Karpati,Tamas;Neumann,Toni;Englert,Ulli;Nyulaszi,Laszlo;Baumgartner,Thomas[Chemistry-AEuropeanJournal,2007,vol.13,#26,p.7487-7500]

[3]Ebner,DavidC.;Bagdanoff,JeffreyT.;Ferreira,EricM.;McFadden,RyanM.;Caspi,DanielD.;Trend,RaissaM.;Stoltz,BrianM.[Chemistry-AEuropeanJournal,2009,vol.15,#47,p.12978-12992]

[4]Browne,DuncanL.;Baumann,Marcus;Harji,BashirH.;Baxendale,IanR.;Ley,StevenV.[OrganicLetters,2011,vol.13,#13,p.3312-3315]

[5]Grisorio,Roberto;Suranna,GianPaolo;Mastrorilli,Piero;Mazzeo,Marco;Colella,Silvia;Carallo,Sonia;Gigli,Giuseppe[DaltonTransactions,2013,vol.42,#24,p.8939-8950]

[1]CurrentPatentAssignee:RENASCIENCE-US2009/124620,2009,A1Locationinpatent:Page/Pagecolumn54

[1]CurrentPatentAssignee:RENASCIENCE-US2009/124620,2009,A1Locationinpatent:Page/Pagecolumn61

[1]Asachenko,AndreyF.;Sorochkina,KristinaR.;Dzhevakov,PavelB.;Topchiy,MaximA.;Nechaev,MikhailS.[AdvancedSynthesisandCatalysis,2013,vol.355,#18,p.3553-3557]

[2]Tan,PengWen;Haughey,Maxwell;Dixon,DarrenJ.[ChemicalCommunications,2015,vol.51,#21,p.4406-4409]

[3]Bower,JohnF.;Cadge,JamieA.;Russell,ChristopherA.;Sparkes,HazelA.[AngewandteChemie-InternationalEdition,2020,vol.59,#16,p.6617-6621][Angew.Chem.,2020,vol.59,p.1-6,6]

[4]Lennox,AlastairJ.J.;Lloyd-Jones,GuyC.[AngewandteChemie-InternationalEdition,2012,vol.51,#37,p.9385-9388]

[5]Erb,William;Albini,Mathieu;Rouden,Jacques;Blanchet,Jrme[JournalofOrganicChemistry,2014,vol.79,#21,p.10568-10580]

[6]Locationinpatent:experimentalpartIsobe,Minoru;Makarasen,Arthit;Kuse,Masaki;Nishikawa,Toshio[BulletinoftheChemicalSocietyofJapan,2009,vol.82,#7,p.870-878]

[7]Fier,PatrickS.;Luo,Jingwei;Hartwig,JohnF.[JournaloftheAmericanChemicalSociety,2013,vol.135,#7,p.2552-2559]

[8]Jiang,Bo;Wu,Songxiao;Zeng,Jing;Yang,Xiaobo[OrganicLetters,2018,vol.20,#20,p.6573-6577]

[9]Demonti,Luca;Mézailles,Nicolas;Nebra,Noel;Saffon-Merceron,Nathalie[Chemistry-AEuropeanJournal,2021,vol.27,#62,p.15396-15405]

Literature
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SDS
Tags:214360-58-4 Molecular Formula|214360-58-4 MDL|214360-58-4 SMILES|214360-58-4 4-Fluorophenylboronic acid, pinacol ester