100524-99-0 Usage
General Description
2-(3-Bromo-2-oxopropyl)-3-methoxy-1-piperidinecarboxylic acid ethyl ester is a chemical compound that belongs to the class of piperidinecarboxylic acid derivatives. It is a synthetic compound with a molecular formula of C12H19BrNO4 and a molecular weight of 315.191 g/mol. 2-(3-Bromo-2-oxopropyl)-3-methoxy-1-piperidinecarboxylic acid ethyl ester is used in the field of medicinal chemistry and drug development, where it may be employed as a building block or intermediate in the synthesis of pharmaceutical compounds. Additionally, it may also have potential applications in research and development activities related to the study of piperidinecarboxylic acid derivatives and their biological activities. Overall, this compound has potential uses in various scientific and industrial applications, particularly in the pharmaceutical and research sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 100524-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,5,2 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 100524-99:
(8*1)+(7*0)+(6*0)+(5*5)+(4*2)+(3*4)+(2*9)+(1*9)=80
80 % 10 = 0
So 100524-99-0 is a valid CAS Registry Number.
100524-99-0Relevant articles and documents
A 2- martonite base -3-methoxy-1-piperidine carboxylic acid ethyl ester preparation method
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Paragraph 0041; 0043, (2017/02/24)
The invention discloses a preparation method for ethyl 2-bromoacetonyl-3-methoxy-1-piperidinecarboxylate. The preparation method comprises the following steps: using a bromination reagent to have a substitution reaction with 2-acetonyl-3-methoxypiperidine, so as to generate 2-bromoacetonyl-3-methoxy-1-piperidine, then reacting 2-bromoacetonyl-3-methoxy-1-piperidine with ethyl chloroformate, so as to synthesize ethyl 2-bromoacetonyl-3-methoxy-1-piperidinecarboxylate. The bromination reagent employed in the method is relatively good in activity and selectivity, and substitution reaction can be performed in a medium polar solvent, so that the reaction difficulty is substantially reduced and the reaction yield is improved. Also the bromination reagent is friendly to environment, does not cause environmental pollution, is cheap and easily available, and helps to substantially reduce cost.