1408168-76-2 Usage
General Description
Potassium trifluoro(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)borate is a chemical compound with the molecular formula K[BF3(C5H10O2)]. It is a boron-based compound that contains potassium, boron, and fluorine atoms. Potassium trifluoro(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)borate is a versatile reagent used in organic synthesis, particularly in the field of organoboron chemistry. It can be used as a reagent for the selective reduction of carbonyl compounds and for the preparation of other organoboron compounds. Additionally, it has applications in the development of pharmaceuticals, agrochemicals, and materials science due to their unique properties and reactivity in various chemical reactions. However, it is important to handle this compound with caution due to its potential reactivity and toxicity.
Check Digit Verification of cas no
The CAS Registry Mumber 1408168-76-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,8,1,6 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1408168-76:
(9*1)+(8*4)+(7*0)+(6*8)+(5*1)+(4*6)+(3*8)+(2*7)+(1*6)=162
162 % 10 = 2
So 1408168-76-2 is a valid CAS Registry Number.
1408168-76-2Relevant articles and documents
TETRAHYDRO-BENZOAZEPINE GLYCOSIDASE INHIBITORS
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Page/Page column 167-168, (2020/03/15)
Compounds of formula (I') wherein A, R1, R2, T1, T2, T3, T4, L, W, Z, R''', m and n have the meaning according to the claims can be employed, inter alia, for the treatment of tauopathies and Alzheimer's disease.
Suzuki-Miyaura cross-coupling of potassium alkoxyethyltrifluoroborates: Access to aryl/heteroarylethyloxy motifs
Fleury-Bregeot, Nicolas,Presset, Marc,Beaumard, Floriane,Colombel, Virginie,Oehlrich, Daniel,Rombouts, Frederik,Molander, Gary A.
, p. 10399 - 10408 (2013/01/15)
The introduction of an alkoxyethyl moiety onto aromatic substructures has remained a long-standing challenge for synthetic organic chemists. The main reasons are the inherent instability of alkoxyethylmetallic species and the lack of general procedures to access them. A new method utilizing a cross-coupling strategy based on the exceptional properties of organotrifluoroborates has been developed, and the method allows an easy and efficient installation of this unit on a broad range of aryl and heteroaryl bromides.
