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Triphenyl borate

CAS No.:
1095-03-0
Catalog Number:
AG0035RM
Molecular Formula:
C18H15BO3
Molecular Weight:
290.1209
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
25g
>96.0%(T)
1 week
United States
$148
- +
500g
>96.0%(T)
1 week
United States
$1146
- +
Product Description
Catalog Number:
AG0035RM
Chemical Name:
Triphenyl borate
CAS Number:
1095-03-0
Molecular Formula:
C18H15BO3
Molecular Weight:
290.1209
MDL Number:
MFCD00059011
IUPAC Name:
triphenyl borate
InChI:
InChI=1S/C18H15BO3/c1-4-10-16(11-5-1)20-19(21-17-12-6-2-7-13-17)22-18-14-8-3-9-15-18/h1-15H
InChI Key:
MDCWDBMBZLORER-UHFFFAOYSA-N
SMILES:
c1ccc(cc1)OB(Oc1ccccc1)Oc1ccccc1
EC Number:
214-137-0
NSC Number:
806
Properties
Complexity:
247  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
290.111g/mol
Formal Charge:
0
Heavy Atom Count:
22  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
290.125g/mol
Monoisotopic Mass:
290.111g/mol
Rotatable Bond Count:
6  
Topological Polar Surface Area:
27.7A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Literature
Title Journal
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. Chirality 20120301
Synthesis and characterization of neutral iron(II) and ruthenium(II) complexes with the isocyanotriphenylborate ligand. Dalton transactions (Cambridge, England : 2003) 20091214
Catalytic asymmetric aziridination with borate catalysts derived from VANOL and VAPOL ligands: scope and mechanistic studies. Chemistry (Weinheim an der Bergstrasse, Germany) 20080101
Direct access to N-H-aziridines from asymmetric catalytic aziridination with borate catalysts derived from vaulted binaphthol and vaulted biphenanthrol ligands. Journal of the American Chemical Society 20070606
An efficient synthesis of (-)-chloramphenicol via asymmetric catalytic aziridination: a comparison of catalysts prepared from triphenylborate and various linear and vaulted biaryls. Organic letters 20011115
Properties