706748-53-0 Usage
General Description
Boronic acid, (1-methyl-4-piperidinyl)- (9CI) is a chemical compound with the molecular formula C10H17BNO2. It belongs to the class of boronic acids, which are known for their use in organic synthesis and medicinal chemistry. This specific compound is a derivative of piperidine, a heterocyclic organic compound commonly found in pharmaceuticals and agrochemicals. Boronic acids have properties that make them useful in the synthesis of pharmaceuticals and other organic compounds due to their ability to form stable complexes with diols and other nucleophiles, making them important in the development of new drugs and materials. The piperidine moiety in this compound suggests potential for use in drugs targeting the central nervous system and other biological applications.
Check Digit Verification of cas no
The CAS Registry Mumber 706748-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,6,7,4 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 706748-53:
(8*7)+(7*0)+(6*6)+(5*7)+(4*4)+(3*8)+(2*5)+(1*3)=180
180 % 10 = 0
So 706748-53-0 is a valid CAS Registry Number.
706748-53-0Relevant articles and documents
Process method for synthesizing N-substituted piperidine-4-boric acid
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Paragraph 0027, (2020/06/17)
The invention relates to an organic compound synthesis method, and relates to a process method for synthesizing N-substituted piperidine-4-boric acid, which comprises the following steps of: reactingN-substituted piperidine-4-alcohol used as a raw material with thionyl chloride and organic alkali in a solvent to generate N-substituted piperidine-4-chlorine, reacting the N-substituted piperidine-4-chlorine used as a raw material with lithium metal and bis (N, N-dimethylamino) borane halide in a solvent, quenching and acidifying to obtain N-substituted piperidine-4-boric acid. The process method has the advantages of originality, low cost, safety and mild reaction conditions, avoids the dangerous reaction that other patented methods adopt expensive palladium hydroxide hydrogenation, has potential cost advantage and safety advantage, and is suitable for industrial scale-up production.
