Potassium (3-methoxyphenyl)trifluoroborate

Product Information

Molecular Formula:
C7H7BF3KO
Molecular Weight:
214.03
Description
Potassium (3-methoxyphenyl)trifluoroborate is a highly prized compound extensively employed within the biomedical domain. It showcases its versatility as a reagent in pharmaceutical synthesis. By virtue of this attribute, it assumes a pivotal function in propelling the advancement of groundbreaking therapies addressing a myriad of maladies such as cancer, inflammation, and neurological malfunctions.
Synonyms
POTASSIUM (3-METHOXYPHENYL)TRIFLUOROBORATE; Potassium (3-methoxypheny)trifluoroborate; POTASSIUM 3-METHOXYPHENYLTRIFLUOROBORAT&
IUPAC Name
potassiumtrifluoro-(3-methoxyphenyl)boranuide
Canonical SMILES
[B-](C1=CC(=CC=C1)OC)(F)(F)F.[K+]
InChI
InChI=1S/C7H7BF3O.K/c1-12-7-4-2-3-6(5-7)8(9,10)11;/h2-5H,1H3;/q-1;+1
InChI Key
GKDCWEPJOSDGHY-UHFFFAOYSA-N
Melting Point
177-180°C(lit.)
Flash Point
Not applicable
Purity
>98.0%(LC)

Safety Information

Hazards
H315 - H319 - H335
Precautionary Statement
P302 + P352 - P305 + P351 + P338

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
5
Rotatable Bond Count
1
Exact Mass
214.0179110 g/mol
Monoisotopic Mass
214.0179110 g/mol
Topological Polar Surface Area
9.2Ų
Heavy Atom Count
13
Formal Charge
0
Complexity
153
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
2
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-113150018-A Four-coordination N, N-chelating monoaryl monofluoroborate compound and preparation method thereof 2021-02-26
CN-111620896-A Preparation method of tetra-coordinated N, N-chelated diaryl borate compound with 8-aminoquinoline derivative as bidentate ligand 2020-06-11
CN-110256306-B Ortho-sulfonamide substituted diaryl iodine compound and preparation method and application thereof 2019-06-27
AU-2015287663-A1 Process for preparing substituted phenylalkanes 2014-07-10
AU-2015287663-B2 Process for preparing substituted phenylalkanes 2014-07-10
CA-2954642-A1 Process for preparing substituted phenylalkanes 2014-07-10
EP-3166923-A1 Process for preparing substituted phenylalkanes 2014-07-10
JP-2017520566-A Process for producing substituted phenylalkanes 2014-07-10
JP-6502397-B2 Method for producing substituted phenyl alkane 2014-07-10
US-2016009635-A1 Process for preparing substituted phenylalkanes 2014-07-10
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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