1408168-76-2 Usage
Uses
Used in Organic Synthesis:
Potassium trifluoro(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)borate is used as a reagent for the selective reduction of carbonyl compounds, which is crucial for the synthesis of various organic compounds.
Used in Organoboron Chemistry:
Potassium trifluoro(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)borate is utilized in the preparation of other organoboron compounds, which are essential building blocks in the synthesis of complex organic molecules.
Used in Pharmaceutical Development:
Potassium trifluoro(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)borate is used as a reagent in the development of pharmaceuticals, owing to its unique properties and reactivity in chemical reactions that can lead to the creation of new drug candidates.
Used in Agrochemical Development:
It is also employed in the development of agrochemicals, where its reactivity can contribute to the synthesis of new compounds for agricultural applications.
Used in Materials Science:
Potassium trifluoro(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)borate has applications in materials science, where its unique properties can be harnessed to develop new materials with specific characteristics.
Used in Research and Development:
Due to its potential reactivity and applications in various chemical reactions, Potassium trifluoro(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)borate is used in research and development settings to explore new synthetic pathways and applications.
It is important to handle Potassium trifluoro(2-((tetrahydro-2H-pyran-2-yl)oxy)ethyl)borate 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 academic research and scientific papers
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.
6,7,8,9-TETRAHYDRO-5H-PYRIDO[2,3-d]AZEPINE DOPAMINE D3 LIGANDS
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Page/Page column 63, (2017/08/30)
The present invention provides compounds of Formula (I): and pharmaceutically acceptable salts thereof wherein the variables R1, R2, R3, R4, R5, a and A are as defined herein; processes for the preparation of; intermediates used in the preparation of; and compositions containing such compounds or salts, and their uses for treating D3-mediated (or D3-associated) disorders including, e.g., substance addiction, substance abuse, schizophrenia (e.g., its cognitive symptoms), cognitive impairment (e.g., cognitive impairment associated with schizophrenia, AD or PD), Parkinson's disease, mania, anxiety, impulse control disorders, sexual disorders and depression.
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.
