948592-78-7 Usage
Uses
Used in Organic Synthesis:
2-(Pyrrolidino)phenylboronic acid is used as a reagent for the formation of carbon-carbon bonds in organic reactions due to its ability to form stable complexes with diols.
Used in Pharmaceutical Research:
2-(Pyrrolidino)phenylboronic acid is used as a reagent for the synthesis of complex organic molecules and pharmaceutical intermediates, owing to its versatility and wide range of applications.
Used in Transition Metal Catalysis:
2-(Pyrrolidino)phenylboronic acid is used as a ligand in transition metal catalysis for various cross-coupling reactions, enabling the formation of new chemical bonds and the synthesis of diverse organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 948592-78-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,8,5,9 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 948592-78:
(8*9)+(7*4)+(6*8)+(5*5)+(4*9)+(3*2)+(2*7)+(1*8)=237
237 % 10 = 7
So 948592-78-7 is a valid CAS Registry Number.
948592-78-7Relevant academic research and scientific papers
Synthesis of novel fused azecine ring systems through application of the tert-amino effect
Dunkel, Petra,Túrós, Gy?rgy,Bényei, Attila,Ludányi, Krisztina,Mátyus, Péter
experimental part, p. 2331 - 2339 (2010/06/12)
Novel fused azecine ring systems were synthesized via the microwave-assisted thermal isomerization of terphenyl or biphenyl-pyridazine compounds possessing a vinyl and a tert-amino group, through application of a new extension of the tert-amino effect. Substrates for the ring closure were prepared from ortho-dihalobenzene or pyridazinone by consecutive Suzuki couplings with ortho-sec-amino- and formylphenylboronic acids, followed by Knoevenagel condensation of the aldehydes obtained.
