Home Indole and Oxindoles 221044-05-9
221044-05-9,MFCD28556906
Catalog No.:AA00BHIL

221044-05-9 | 1-(Pyrimidin-2-yl)-1h-indole

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100mg
98%
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$27.00   $19.00
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250mg
98%
in stock  
$51.00   $36.00
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1g
98%
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$90.00   $63.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
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  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00BHIL
Chemical Name:
1-(Pyrimidin-2-yl)-1h-indole
CAS Number:
221044-05-9
Molecular Formula:
C12H9N3
Molecular Weight:
195.2200
MDL Number:
MFCD28556906
SMILES:
c1cnc(nc1)n1ccc2c1cccc2
Properties
Computed Properties
 
Complexity:
213  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
2  
Rotatable Bond Count:
1  
XLogP3:
3  

Downstream Synthesis Route

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[2]Patent:CN112574180,2021,A.Locationinpatent:Paragraph0047

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[10]JournalofMolecularStructure,2022,vol.1247

[11]OrganicLetters,2019,vol.21,p.4077-4081

[12]OrganicandBiomolecularChemistry,2021,vol.19,p.2949-2958

[13]OrganicandBiomolecularChemistry,2012,vol.10,p.8953-8955

[14]RSCAdvances,2015,vol.5,p.39358-39365

[15]OrganicandBiomolecularChemistry,2017,vol.15,p.536-540

[16]Patent:CN112979648,2021,A.Locationinpatent:Paragraph0061-0067

[17]Patent:JP2017/171619,2017,A.Locationinpatent:Paragraph0267;0268

[18]Synthesis,2008,p.1707-1716

[19]OrganicLetters,2020,vol.22,p.4097-4102

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[22]OrganicLetters,2013,vol.15,p.1290-1293

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[28]OrganicandBiomolecularChemistry,2015,vol.13,p.9000-9004

[29]TetrahedronLetters,2016,vol.57,p.1728-1731

[30]Patent:CN105622585,2016,A.Locationinpatent:Paragraph0016;0036;0039

[31]EuropeanJournalofOrganicChemistry,2016,vol.2016,p.5637-5641

[32]Patent:CN106279236,2017,A.Locationinpatent:Paragraph0042;0043;0044;0045;0074;0075-0103

[33]ChemicalCommunications,2017,vol.53,p.8731-8734

[34]OrganicLetters,2017,vol.19,p.6164-6167

[35]Patent:CN106279116,2017,A.Locationinpatent:Paragraph0040;0042

[36]JournaloftheAmericanChemicalSociety,2018,vol.140,p.586-589

[37]OrganicandBiomolecularChemistry,2018,vol.16,p.7174-7177

[38]Patent:CN109232606,2019,A.Locationinpatent:Paragraph0063;0064;0065

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[40]OrganicLetters,2020,vol.22,p.2663-2668

[41]OrganicLetters,2021,vol.23,p.5545-5548

[42]OrganicLetters,2021,vol.23,p.5719-5723

[43]EuropeanJournalofOrganicChemistry,2021,vol.2021,p.4938-4942

[1]EuropeanJournalofOrganicChemistry,2021,vol.2021,p.4938-4942

[2]OrganicLetters,2011,vol.13,p.3332-3335

[3]AngewandteChemie-InternationalEdition,2017,vol.56,p.3172-3176    Angew.Chem.,2017,vol.129,p.3220-3224,5

[4]AngewandteChemie-InternationalEdition,2017,vol.56,p.6339-6342    Angew.Chem.,2017,vol.129,p.6436-6439

[5]OrganicLetters,2021,vol.23,p.1960-1965

[6]ACSCatalysis,2017,vol.7,p.2511-2515

[7]EuropeanJournalofOrganicChemistry,2021,vol.2021,p.5507-5517

[8]Chemistry-AEuropeanJournal,2013,vol.19,p.9142-9146

[9]ChemicalCommunications,2015,vol.51,p.2925-2928

[10]Chemistry-AEuropeanJournal,2015,vol.21,p.5380-5386

[11]OrganicLetters,2018,vol.20,p.341-344

[12]JournalofOrganicChemistry,2017,vol.82,p.10665-10672

[13]AngewandteChemie-InternationalEdition,2020,vol.59,p.23537-23543    AngewandteChemie,2020,vol.132,p.23743-23749,7

[1]AngewandteChemie-InternationalEdition,2012,vol.51,p.6993-6997

[1]AngewandteChemie-InternationalEdition,2012,vol.51,p.6993-6997

[2]ScienceChinaChemistry,2018,vol.61,p.200-205

[1]ScienceChinaChemistry,2018,vol.61,p.200-205

[2]AngewandteChemie-InternationalEdition,2012,vol.51,p.6993-6997

Literature

Title: C2-Alkylation of N-pyrimidylindole with vinylsilane via cobalt-catalyzed C-H bond activation.

Journal: Beilstein journal of organic chemistry 20120101

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