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1095-03-0,MFCD00059011
Catalog No.:AA0035OU

1095-03-0 | Triphenyl borate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
>95.0%
in stock  
$93.00   $65.00
- +
25g
>95.0%
in stock  
$190.00   $133.00
- +
100g
>95.0%
in stock  
$461.00   $323.00
- +
500g
>96.0%(T)
in stock  
$1,023.00   $716.00
- +
  • Technical Information
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA0035OU
Chemical Name:
Triphenyl borate
CAS Number:
1095-03-0
Molecular Formula:
C18H15BO3
Molecular Weight:
290.1209
MDL Number:
MFCD00059011
SMILES:
c1ccc(cc1)OB(Oc1ccccc1)Oc1ccccc1
NSC Number:
806
Properties
Properties
 
BP:
158°C/0.05mmHg(lit.)  
Form:
Solid  
MP:
98-101 °C(lit.)  
Solubility:
Soluble in chloroform, methanol.  
Stability:
Moisture Sensitive  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
247  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
22  
Hydrogen Bond Acceptor Count:
3  
Rotatable Bond Count:
6  

Literature

Title: First isolation of disubstituted cis-5,6-dihydro-1,10-phenanthrolines. Lipase-mediated resolution of cis- and trans-phenoxy alcohol isomers and assignment of absolute stereochemistry via CD and NMR spectroscopy.

Journal: Chirality 20120301

Title: Synthesis and characterization of neutral iron(II) and ruthenium(II) complexes with the isocyanotriphenylborate ligand.

Journal: Dalton transactions (Cambridge, England : 2003) 20091214

Title: Catalytic asymmetric aziridination with borate catalysts derived from VANOL and VAPOL ligands: scope and mechanistic studies.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20080101

Title: Direct access to N-H-aziridines from asymmetric catalytic aziridination with borate catalysts derived from vaulted binaphthol and vaulted biphenanthrol ligands.

Journal: Journal of the American Chemical Society 20070606

Title: An efficient synthesis of (-)-chloramphenicol via asymmetric catalytic aziridination: a comparison of catalysts prepared from triphenylborate and various linear and vaulted biaryls.

Journal: Organic letters 20011115

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