Home Boronic Acids 419536-33-7
419536-33-7,MFCD13176534
Catalog No.:AA00BXOB

419536-33-7 | 4-(9H-Carbozol-9-yl)phenylboronic acid

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1g
98%
in stock  
$7.00   $5.00
- +
5g
98%
in stock  
$12.00   $8.00
- +
10g
98%
in stock  
$22.00   $15.00
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25g
98%
in stock  
$44.00   $31.00
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100g
98%
in stock  
$173.00   $121.00
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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:
AA00BXOB
Chemical Name:
4-(9H-Carbozol-9-yl)phenylboronic acid
CAS Number:
419536-33-7
Molecular Formula:
C18H14BNO2
Molecular Weight:
287.1203
MDL Number:
MFCD13176534
SMILES:
OB(c1ccc(cc1)n1c2ccccc2c2c1cccc2)O
Properties
Computed Properties
 
Complexity:
361  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
22  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
2  

Upstream Synthesis Route

[1]JournalofMaterialsChemistryC,2018,vol.6,#32,p.8733-8737

[1]OrganicandBiomolecularChemistry,2012,vol.10,#33,p.6693-6704

[2]AustralianJournalofChemistry,2007,vol.60,#8,p.603-607

[3]PhysicalChemistryChemicalPhysics,2011,vol.13,#39,p.17825-17830

[4]OrganicandBiomolecularChemistry,2012,vol.10,#47,p.9481-9490

[5]Patent:WO2013/12297,2013,A1,.Locationinpatent:Paragraph111;114;115

[6]InorganicaChimicaActa,2011,vol.370,#1,p.340-345

[7]Patent:US8093399,2012,B2,.Locationinpatent:Page/Pagecolumn107

[8]Patent:US7758972,2010,B2,.Locationinpatent:Page/Pagecolumn78;79

[9]Patent:WO2011/14039,2011,A1,.Locationinpatent:Page/Pagecolumn20;21

[10]InorganicaChimicaActa,2012,vol.391,p.50-57

[11]ChemistryLetters,2008,vol.37,#3,p.262-263

[12]AdvancedFunctionalMaterials,2010,vol.20,#15,p.2448-2458

[13]JournalofMaterialsChemistry,2012,vol.22,#37,p.19700-19708,9

[14]JournalofMaterialsChemistry,2012,vol.22,#37,p.19700-19708

[1]ChemicalCommunications,2013,vol.49,#34,p.3597-3599

[2]JournaloftheChileanChemicalSociety,2015,vol.60,#2,p.2971-2974

[3]InorganicaChimicaActa,2011,vol.370,#1,p.340-345

[4]Patent:CN103588770,2016,B,.Locationinpatent:Paragraph0052

[5]JournalofMaterialsChemistryC,2015,vol.3,#22,p.5835-5843

[6]Patent:WO2008/26614,2008,A1,.Locationinpatent:Page/Pagecolumn76-77

[7]Patent:CN106243086,2016,A,.Locationinpatent:Paragraph0012

[8]Patent:EP1972619,2008,A1,.Locationinpatent:Page/Pagecolumn282

[9]Patent:US2008/145700,2008,A1,

[10]ChemistryLetters,2008,vol.37,#3,p.262-263

[11]OrganicandBiomolecularChemistry,2012,vol.10,#33,p.6693-6704

[12]DyesandPigments,2013,vol.96,#3,p.705-713

[13]Patent:EP2857395,2015,A1,.Locationinpatent:Paragraph0105

[14]TurkishJournalofChemistry,2015,vol.39,#5,p.917-929

[15]ChemistryofHeterocyclicCompounds,2016,vol.52,#6,p.379-387

[16]Khim.Geterotsikl.Soedin.,2016,vol.52,#6,p.379-387,9

[1]JournalofMaterialsChemistryC,2014,vol.2,#46,p.9858-9865

[2]AngewandteChemie-InternationalEdition,2014,vol.53,#19,p.4850-4855

[3]Angew.Chem.,2014,vol.126,#19,p.4950-4955,6

[4]AngewandteChemie-InternationalEdition,2016,vol.55,#9,p.3049-3053

[5]Angew.Chem.,2016,vol.128,#9,p.3101-3105,5

[6]DyesandPigments,2017,vol.142,p.175-182

[7]DyesandPigments,2016,vol.129,p.34-42

[8]Patent:KR2015/29332,2015,A,.Locationinpatent:Paragraph0052;0066;0067

[9]Patent:KR2015/29331,2015,A,.Locationinpatent:Paragraph0055;0066;0067

[1]Patent:CN105585577,2016,A,.Locationinpatent:Paragraph0225;0026;0227;0228

Downstream Synthesis Route

[1]Patent:WO2007/125934,2007,A1.Locationinpatent:Page/Pagecolumn198-199

[2]Patent:US8288012,2012,B2.Locationinpatent:Page/Pagecolumn181-182

[3]Patent:KR2015/24803,2015,A.Locationinpatent:Paragraph0212-0214

[1]Patent:WO2008/26614,2008,A1.Locationinpatent:Page/Pagecolumn77-78

419536-33-7    400607-05-8   
9-(biphenyl-4-yl)-10-4-(carbazol-9-yl)phenylanthracene 

[1]Patent:WO2008/26614,2008,A1.Locationinpatent:Page/Pagecolumn83-84

419536-33-7   
9-bromo-10-(4-trifluoromethylphenyl)anthracene 
 
9-4-(carbazol-9-yl)phenyl-10-(4-trifluoromethylphenyl)anthracene 

[1]Patent:WO2008/26614,2008,A1.Locationinpatent:Page/Pagecolumn97-98

419536-33-7    474688-73-8   
9-(4-(10-(naphthalen-2-yl)anthracen-9-yl)phenyl)-9H-carbazole 

[1]Patent:WO2008/26614,2008,A1.Locationinpatent:Page/Pagecolumn103-104

Literature

Title: A highly efficient and aerobic protocol for the synthesis of N-heteroaryl substituted 9-arylcarbazolyl derivatives via a palladium-catalyzed ligand-free Suzuki reaction.

Journal: Organic & biomolecular chemistry 20121021

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