Catalog No.:AA00E94M

58861-53-3 | 2-(4-Fluorophenyl)pyridine

Name: Name:2-(4-Fluorophenyl)pyridine
Brand: AABLOCKS
SKU: AA00E94M
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100mg

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$9.00 $7.00

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250mg

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$12.00 $8.00

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95%

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$14.00 $10.00

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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature
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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA00E94M

Chemical Name:

2-(4-Fluorophenyl)pyridine

CAS Number:

58861-53-3

Molecular Formula:

C11H8FN

Molecular Weight:

173.1863

MDL Number:

MFCD06201382

SMILES:

Fc1ccc(cc1)c1ccccn1

Properties

Computed Properties

Complexity:

152

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

XLogP3:

2.7

Upstream Synthesis Route

58861-53-3

33421-36-2

1452876-10-6

[1]ACSCatalysis,2016,vol.6,#9,p.6050-6054

58861-53-3

33421-36-2

1452876-10-6

[1]AngewandteChemie-InternationalEdition,2013,vol.52,#22,p.5827-5831

[2]Angew.Chem.,2013,vol.125,#22,p.5939-5943,5

Downstream Synthesis Route

58861-53-3

10025-83-9

fac-tris(F(C6H4)pyridine)iridium

[1]ChemicalCommunications,2001,p.1494-1495

58861-53-3

71-41-0

201230-82-2

1101187-17-0

[1]JournaloftheAmericanChemicalSociety,2009,vol.131,p.729-733

109-04-6

1765-93-1

58861-53-3

[1]EuropeanJournalofOrganicChemistry,2010,p.5548-5551

[2]OrganicandBiomolecularChemistry,2011,vol.9,p.1054-1060

[3]OrganicandBiomolecularChemistry,2012,vol.10,p.7875-7883

[4]ChemicalCommunications,2009,p.6267-6269

[5]OrganicandBiomolecularChemistry,2013,vol.11,p.2756-2760

[6]ChemicalCommunications,2015,vol.51,p.12807-12810

[7]OrganicandBiomolecularChemistry,2017,vol.15,p.5993-6000

[8]AdvancedSynthesisandCatalysis,2018,vol.360,p.3990-3998

[9]Tetrahedron,2019,vol.75,p.2547-2552

[10]JournalofMaterialsChemistryA,2014,vol.2,p.15945-15951

[11]EuropeanJournalofInorganicChemistry,2016,vol.2016,p.5044-5051

[12]InorganicaChimicaActa,2018,vol.477,p.227-232

[13]DaltonTransactions,2018,vol.47,p.17202-17205

[14]Organometallics,2015,vol.34,p.2683-2694

[15]GreenChemistry,2011,vol.13,p.1260-1266

[16]CuihuaXuebao/ChineseJournalofCatalysis,2014,vol.35,p.357-361

[17]JournaloftheAmericanChemicalSociety,2013,vol.135,p.4771-4787

[18]JournaloftheAmericanChemicalSociety,2017,vol.139,p.8267-8276

[19]OrganicLetters,2009,vol.11,p.3974-3977

[20]AdvancedSynthesisandCatalysis,2010,vol.352,p.632-636

[21]JournaloftheAmericanChemicalSociety,2010,vol.132,p.10272-10274

[22]JournaloftheAmericanChemicalSociety,2012,vol.134,p.9110-9113

[23]OrganicLetters,2012,vol.14,p.4594-4597

[24]JournaloftheAmericanChemicalSociety,2013,vol.135,p.9322-9325

[25]JournalofOrganicChemistry,2014,vol.79,p.4414-4422

[26]OrganicLetters,2014,vol.16,p.2661-2663

[27]OrganicLetters,2015,vol.17,p.660-663

[28]OrganicLetters,2015,vol.17,p.1513-1516

[29]AngewandteChemie-InternationalEdition,2015,vol.54,p.4508-4511 Angew.Chem.,2015,vol.127,p.4591-4594,4

[30]JournalofOrganicChemistry,2015,vol.80,p.4116-4122

[31]NewJournalofChemistry,2015,vol.39,p.5259-5264

[32]RSCAdvances,2015,vol.5,p.42815-42827

[33]TetrahedronLetters,2015,vol.56,p.6136-6141

[34]AngewandteChemie-InternationalEdition,2015,vol.54,p.11677-11680 Angew.Chem.,2015,vol.127,p.11843-11846,4

[35]TetrahedronLetters,2016,vol.57,p.90-94

[36]AngewandteChemie-InternationalEdition,2015,vol.54,p.15284-15288 Angew.Chem.,2015,vol.127,p.15499-15503,5

[37]Synthesis,2016,vol.48,p.1616-1621

[38]OrganicLetters,2017,vol.19,p.1216-1219

[39]Chemistry-AEuropeanJournal,2017,vol.23,p.3285-3290

[40]ChemicalCommunications,2017,vol.53,p.7994-7997

[41]OrganicandBiomolecularChemistry,2017,vol.15,p.6592-6603

[42]OrganicLetters,2018,vol.20,p.5533-5536

[43]OrganicLetters,2019,vol.21,p.3735-3740

[44]ChemicalScience,2019,vol.10,p.7898-7906

[45]Tetrahedron,2019,vol.75

58861-53-3

1206523-63-8

[1]AdvancedSynthesisandCatalysis,2009,vol.351,p.2071-2074

[2]Synthesis,2016,vol.48,p.1616-1621

[3]Tetrahedron,2020

[4]JournaloftheAmericanChemicalSociety,2019,vol.141,p.18630-18640

109-09-1

1765-93-1

58861-53-3

[1]JournalofOrganometallicChemistry,2015,vol.776,p.51-59

[2]OrganicandBiomolecularChemistry,2017,vol.15,p.3924-3929

[3]DaltonTransactions,2013,vol.42,p.6859-6866

[4]Synthesis,2009,p.3094-3098

[5]JournalofOrganicChemistry,2016,vol.81,p.6988-6994

[6]InorganicaChimicaActa,2018,vol.477,p.227-232

[7]JournaloftheIranianChemicalSociety,2016,vol.13,p.637-644

Literature

Title: 4-[5-Amino-4-(4-fluoro-phen-yl)-3-(pyridin-4-yl)-1H-pyrazol-1-yl]benzo-nitrile.

Journal: Acta crystallographica. Section E, Structure reports online 20120401

Title: 4-(4-Fluoro-phen-yl)-1-phenyl-3-(pyridin-4-yl)-1H-pyrazol-5-amine.

Journal: Acta crystallographica. Section E, Structure reports online 20120301

Title: 4-(4-Fluoro-phen-yl)-1-(4-nitro-phen-yl)-3-(pyridin-4-yl)-1H-pyrazol-5-amine.

Journal: Acta crystallographica. Section E, Structure reports online 20120301

Title: Efficient blue-emitting Ir(III) complexes with phosphine carbanion-based ancillary ligand: a DFT study.

Journal: The journal of physical chemistry. A 20111027

Title: Diphenyl(1-naphthyl)phosphine ancillary for assembling of red and orange-emitting Ir(III) based phosphors; strategic synthesis, photophysics, and organic light-emitting diode fabrication.

Journal: Inorganic chemistry 20101004

Title: 5-(4-Fluoro-phen-yl)-4-(4-pyrid-yl)-1,3-oxazol-2-amine.

Journal: Acta crystallographica. Section E, Structure reports online 20100401

Title: tert-Butyl N-benzyl-N-[4-(4-fluoro-benzoyl-meth-yl)-2-pyrid-yl]carbamate.

Journal: Acta crystallographica. Section E, Structure reports online 20081101

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