948592-78-7 Usage
General Description
2-(Pyrrolidino)phenylboronic acid is a chemical compound that is commonly used in organic synthesis and pharmaceutical research. It consists of a boronic acid group attached to a phenyl ring with a pyrrolidino group. 2-(Pyrrolidino)phenylboronic acid is known for its ability to form stable complexes with diols, making it useful in the formation of carbon-carbon bonds in organic reactions. Its boronic acid group also allows it to act as a ligand in transition metal catalysis, enabling it to participate in various cross-coupling reactions. It is often used as a reagent for the synthesis of complex organic molecules and pharmaceutical intermediates due to its versatility and wide range of applications.
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 articles and documents
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.
