DIMESITYLBORON FLUORIDE

Product Information

Molecular Formula:
C18H22BF
Molecular Weight:
268.18
Description
DIMESITYLBORON FLUORIDE is a prominent reagent extensively utilized in the realm of biomedicine. It exhibits exceptional characteristics that render it highly suitable for a myriad of applications encompassing drug synthesis. Particularly noteworthy is its profound significance in combating conditions such as cancer, diabetes, neurodegenerative diseases, and inflammatory disorders. The compound assumes a pivotal role in augmenting the efficacy of targeted drug delivery systems while concurrently facilitating the conception of pioneering therapeutic approaches tailored specifically for these afflictions.
Synonyms
Dimesitylboron Fluoride
IUPAC Name
fluoro-bis(2,4,6-trimethylphenyl)borane
Canonical SMILES
B(C1=C(C=C(C=C1C)C)C)(C2=C(C=C(C=C2C)C)C)F
InChI
InChI=1S/C18H22BF/c1-11-7-13(3)17(14(4)8-11)19(20)18-15(5)9-12(2)10-16(18)6/h7-10H,1-6H3
InChI Key
WZWGERGANZMXOM-UHFFFAOYSA-N
Melting Point
69-72 °C (lit.)
Flash Point
Not applicable
Purity
>98.0%(LC)

Safety Information

Hazards
H314
Precautionary Statement
P280 - P305 + P351 + P338 - P310

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
2
Exact Mass
268.1798590 g/mol
Monoisotopic Mass
268.1798590 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
20
Formal Charge
0
Complexity
265
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
KR-102283490-B1 Light-emitting material for organic electroluminescent device, organic electroluminescent device using same, and material for organic electroluminescent device 2021-01-07
CN-112279851-A Ullazine derivative containing diaryl boron and diaryl amine and synthetic method thereof 2020-09-28
US-2022056062-A1 Organic electroluminescent materials and devices 2020-08-19
WO-2021224368-A1 Organic molecules for optoelectronic devices 2020-05-06
KR-20210081139-A Compound, Organic EL Device and Display Device 2019-12-23
TW-202124397-A Compound, organic el device and display device 2019-12-23
WO-2021132952-A1 Compound, organic electroluminescent element, and display device 2019-12-23
KR-102341068-B1 Compound, Organic EL Device and Display Device 2019-12-23
KR-20210076428-A Compound, Organic EL Device and Display Device 2019-12-16
TW-202124391-A Compound, organic el device and display device 2019-12-16

Literatures

PMID Publication Date Title Journal
22259501 2012-01-01 2,8-Dimesitylboranyl-6H,12H-5,11-methano-dibenzo[b,f][1,5]diazo-cine Acta crystallographica. Section E, Structure reports online
20967328 2010-12-07 Reactivity of the bifunctional ambiphilic molecule 8-(dimesitylboryl)quinoline: hydrolysis and coordination to Cu(I), Ag(I) and Pd(II) Dalton transactions (Cambridge, England : 2003)
21582141 2009-02-06 Oxybis(dimesitylborane) dichloro-methane hemisolvate Acta crystallographica. Section E, Structure reports online
21581783 2009-01-14 Bis(μ-dimesitylborinato-κO:O)bis-[(2-methyl-pyridine-κN)lithium] Acta crystallographica. Section E, Structure reports online
18327943 2008-04-02 Synthesis of B/Si bidentate Lewis acids, o-(Fluorosilyl)(dimesitylboryl)benzenes, and their fluoride ion affinity Journal of the American Chemical Society
16429474 2006-03-20 Synthesis, crystal structures, linear and nonlinear optical properties, and theoretical studies of (p-R-phenyl)-, (p-R-phenylethynyl)-, and (E)-[2-(p-R-phenyl)ethenyl]dimesitylboranes and related compounds Chemistry (Weinheim an der Bergstrasse, Germany)
12203306 2002-08-16 Synthesis of B/Ga and B/In heteronuclear bidentate Lewis acids: formation of intramolecular pi-arene-gallium(III) and -indium(III) complexes Chemistry (Weinheim an der Bergstrasse, Germany)
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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