Home Boronic Acids 68716-49-4
68716-49-4,MFCD11110553
Catalog No.:AA0036JO

68716-49-4 | 4-Bromophenylboronic acid, pinacol ester

Pack Size
Purity
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Price(USD)
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250mg
98%
in stock  
$6.00   $4.00
- +
1g
98%
in stock  
$7.00   $5.00
- +
5g
98%
in stock  
$11.00   $8.00
- +
10g
98%
in stock  
$18.00   $13.00
- +
25g
98%
in stock  
$44.00   $31.00
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100g
96%
in stock  
$147.00   $103.00
- +
500g
96%
in stock  
$685.00   $480.00
- +
  • 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:
AA0036JO
Chemical Name:
4-Bromophenylboronic acid, pinacol ester
CAS Number:
68716-49-4
Molecular Formula:
C12H16BBrO2
Molecular Weight:
282.9692
MDL Number:
MFCD11110553
SMILES:
CC1(C)OB(OC1(C)C)c1ccc(cc1)Br
Properties
Properties
 
BP:
324.1°C at 760 mmHg  
Form:
Solid  
MP:
69.0 to 73.0 °C  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
244  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
2  
Rotatable Bond Count:
1  

Upstream Synthesis Route

[1]Patent:TWI614236,2018,B,.Locationinpatent:Paragraph0122;0123

[1]OrganicLetters,2010,vol.12,#23,p.5474-5477

[1]ChemicalCommunications,2015,vol.51,#14,p.2878-2881

[1]ChemicalCommunications,2015,vol.51,#14,p.2878-2881

[1]ChemicalCommunications,2015,vol.51,#14,p.2878-2881

Downstream Synthesis Route

[1]OrganicLetters,2003,vol.5,p.4635-4638

[2]TetrahedronLetters,2000,vol.41,p.8683-8686

[3]AdvancedSynthesisandCatalysis,2012,vol.354,p.2625-2628

[4]BeilsteinJournalofOrganicChemistry,2014,vol.10,p.981-989

[5]ChemicalCommunications,2019,vol.55,p.6201-6204

[6]ChemSusChem,2020,vol.13,p.1715-1719

[7]ChemistryOpen,2017,vol.6,p.345-349

[8]BeilsteinJournalofOrganicChemistry,2017,vol.13,p.1463-1469

[9]Science,2019,vol.366,p.1500-1504

[1]JournalofOrganometallicChemistry,2001,vol.640,p.197-199

[2]JournalofOrganometallicChemistry,2001,vol.640,p.197-199

[3]OrganicLetters,2006,vol.8,p.261-263

[4]ChemicalCommunications,2002,p.1566-1567

[5]AngewandteChemie-InternationalEdition,2002,vol.41,p.563-572

[6]Patent:US6680401,2004,B1.Locationinpatent:Pagecolumn70

[1]Patent:WO2006/122117,2006,A2.Locationinpatent:Page/Pagecolumn23

[2]TetrahedronLetters,2002,vol.43,p.5965-5968

[3]ChemicalCommunications,2015,vol.51,p.2878-2881

[4]OrganicLetters,2010,vol.12,p.3216-3218

[5]Chemistry-AEuropeanJournal,2019,vol.25,p.16550-16554

[6]AngewandteChemie-InternationalEdition,2017,vol.56,p.7078-7082    Angew.Chem.,2017,vol.129,p.7184-7188,5

[7]JournaloftheAmericanChemicalSociety,2017,vol.139,p.3153-3160

[8]AngewandteChemie-InternationalEdition,2019,vol.58,p.592-595    Angew.Chem.,2019,vol.131,p.602-605,4

[9]JournalofOrganicChemistry,2007,vol.72,p.6618-6620

[10]OrganicLetters,2005,vol.7,p.5191-5194

[11]Patent:WO2006/86562,2006,A2.Locationinpatent:Page/Pagecolumn252

[12]JournaloftheAmericanChemicalSociety,2013,vol.135,p.2552-2559

[13]Patent:WO2006/102674,2006,A2.Locationinpatent:Page/Pagecolumn254-255;284

[14]Patent:WO2006/122186,2006,A2.Locationinpatent:Page/Pagecolumn225

[15]Patent:WO2006/121861,2006,A2.Locationinpatent:Page/Pagecolumn181-182

[16]Patent:CN111004149,2020,A.Locationinpatent:Paragraph0023-0026

623-00-7    4187-87-5    68716-49-4   
4'-(3-oxo-3-phenyl-propenyl)-biphenyl-4-carbonitrile 

[1]Synlett,2006,p.3469-3473

4187-87-5    68716-49-4   
(E)-1-phenyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)prop-2-en-1-one 

[1]Synlett,2006,p.3469-3473

[2]JournalofMedicinalChemistry,2019,vol.62,p.3447-3474

Literature
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