Potassium Allyltrifluoroborate

Product Information

Molecular Formula:
C3H5F3BK
Molecular Weight:
147.98
Description
Organotrifluoroborate involved in: Catalytic allylboration; Stereoselective nucleophilic addition; Pd-catalyzed heterocyclizations; Oxidation reactions and Oxidative Mannich reactions; Cross-coupling reactionsOrganotrifluoroborates as versatile and stable boronic acid surrogates.
Synonyms
potassium;trifluoro(prop-2-enyl)boranuide; potassium;trifluoro(prop-2-enyl)boranuide
IUPAC Name
potassium;trifluoro(prop-2-enyl)boranuide
Canonical SMILES
[B-](CC=C)(F)(F)F.[K+]
InChI
InChI=1S/C3H5BF3.K/c1-2-3-4(5,6)7;/h2H,1,3H2;/q-1;+1
InChI Key
TVPZAMJXLCDMIT-UHFFFAOYSA-N
Melting Point
>300 °C
Flash Point
Not applicable
Purity
95 %
LogP
2.01980

Safety Information

Hazards
H315 - H318 - H335
Precautionary Statement
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P310, P312, P321, P332+P313, P362, P403+P233, P405, and P501
Signal Word
Danger

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
1
Exact Mass
148.0073463 g/mol
Monoisotopic Mass
148.0073463 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
8
Formal Charge
0
Complexity
69.4
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
WO-2022047145-A1 Rapidly accelerating fibrosarcoma protein degrading compounds and associated methods of use 2020-08-28
WO-2022040799-A1 Antimicrobial composition 2020-08-27
WO-2021127743-A1 Substituted hydroxystilbene compounds and derivatives synthesis and uses thereof 2019-12-23
WO-2021086833-A1 Small molecule inhibitors of kras g12c mutant 2019-10-28
TW-202130645-A Small molecule inhibitors of kras g12c mutant 2019-10-28
WO-2019204537-A1 N-[4-oxo-2,3-dihydro-1,5-benzoxazepin-3-yl]-5,6-dihydro-4h-pyrrolo[1,2-b]pyrazol e-2-carboxamide derivatives and related compounds as rip1 kinase inhibitors for treating e.g. irritable bowel syndrome (ibs) 2018-04-20
CN-112074519-A N- [ 4-oxo-2, 3-dihydro-1, 5-benzoxazepin-3-yl ] -5, 6-dihydro-4H-pyrrolo [1,2-B ] pyrazole-2-carboxamide derivatives and related compounds as RIP1 kinase inhibitors for the treatment of e.g. Irritable Bowel Syndrome (IBS) 2018-04-20
EP-3781571-A1 N-[4-oxo-2,3-dihydro-1,5-benzoxazepin-3-yl]-5,6-dihydro-4h-pyrrolo[1,2-b]pyrazol e-2-carboxamide derivatives and related compounds as rip1 kinase inhibitors for treating e.g. irritable bowel syndrome (ibs) 2018-04-20
US-2021032271-A1 Pyridine lactam compounds and methods of use thereof 2018-04-20
JP-2021522206-A N- [4-oxo-2,3-dihydro-1,5-benzoxazepine-3-yl] -5,6-dihydro-4H-pyrrolo [1,2-b] pyrazole-2-carboxamide derivative and Related compounds as RIP1 kinase inhibitors for the treatment of irritable bowel syndrome (IBS), for example 2018-04-20
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

Related Products

Online Inquiry
  • Verification code
USA
  • International:
  • US & Canada (Toll free):
  • Email:
  • Fax:
UK
  • Email:
Copyright © 2024 BOC Sciences. All rights reserved.
Top
Inquiry Basket