706748-53-0 Usage
Uses
Used in Organic Synthesis:
Boronic acid, (1-methyl-4-piperidinyl)(9CI) is used as a reagent in organic synthesis for the formation of stable complexes with diols and other nucleophiles. This property makes it an important component in the synthesis of pharmaceuticals and other organic compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Boronic acid, (1-methyl-4-piperidinyl)(9CI) is used as a building block for the development of new drugs. Its ability to form stable complexes with various biomolecules allows for the design of compounds with specific biological activities.
Used in Drug Development for Central Nervous System:
Boronic acid, (1-methyl-4-piperidinyl)(9CI) is used as a potential drug candidate for targeting the central nervous system. The presence of the piperidine moiety in Boronic acid, (1-methyl-4-piperidinyl)- (9CI) suggests its potential use in the development of drugs that can modulate neurotransmission and treat neurological disorders.
Used in Agrochemicals:
In the agrochemical industry, Boronic acid, (1-methyl-piperidinyl)(9CI) is used as a component in the development of new pesticides and other agrochemicals. Its ability to form stable complexes with various molecules can be utilized to create compounds with specific pesticidal properties.
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 academic research and scientific papers
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.
