592-39-2 Usage
Uses
Used in Pharmaceutical Industry:
Boron Trifluoride Piperidine Complex is used as a catalyst for the synthesis of pharmaceutical compounds. It facilitates a range of chemical reactions, such as acylations and alkylations, which are crucial in the production of various drugs.
Used in Agrochemical Industry:
In the agrochemical sector, Boron Trifluoride Piperidine Complex serves as a catalyst for the synthesis of agrochemicals. Its ability to catalyze reactions like polymerizations helps in the development of effective agricultural chemicals.
Used in Polymer Industry:
Boron Trifluoride Piperidine Complex is utilized as a catalyst in the polymer industry for the production of different types of polymers. Its high reactivity and selectivity are essential in the synthesis of polymers with specific properties.
It is important to handle Boron Trifluoride Piperidine Complex with care due to its corrosive nature and potential to emit toxic fumes if mishandled. Proper safety measures should be taken to ensure the safe use of this complex in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 592-39-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 592-39:
(5*5)+(4*9)+(3*2)+(2*3)+(1*9)=82
82 % 10 = 2
So 592-39-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H11N.BF3/c1-2-4-6-5-3-1;2-1(3)4/h6H,1-5H2;
592-39-2Relevant academic research and scientific papers
Remote Oxidation of Aliphatic C-H Bonds in Nitrogen-Containing Molecules
Howell, Jennifer M.,Feng, Kaibo,Clark, Joseph R.,Trzepkowski, Louis J.,White, M. Christina
supporting information, p. 14590 - 14593 (2015/12/08)
Nitrogen heterocycles are ubiquitous in natural products and pharmaceuticals. Herein, we disclose a nitrogen complexation strategy that employs a strong Bronsted acid (HBF4) or an azaphilic Lewis acid (BF3) to enable remote, non-directed C(sp3)-H oxidations of tertiary, secondary, and primary amine- and pyridine-containing molecules with tunable iron catalysts. Imides resist oxidation and promote remote functionalization.
Multinuclear NMR spectra, 1H-T1 relaxation, conformational behavior, and intramolecular Hδ-····δ+H contacts of N-borane cyclic adducts in solution
Gueizado-Rodriguez,Flores-Parra,Sanchez-Ruiz,Tapia-Benavides,Contreras,Bakhmutov
, p. 3243 - 3246 (2008/10/08)
The VT 1H NMR and 1H-NOESY spectra revealed "frozen" envelope conformations in solutions of 1 and 2 with the BR3 groups in equatorial positions. The 1H-T1 relaxation measurements provided determinatio
