45266-20-4 Usage
Uses
Used in Chemical Applications:
2,9-dibutyldecanedioic acid is used as a chemical intermediate for the synthesis of various compounds. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable component in the production of specialty chemicals.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, 2,9-dibutyldecanedioic acid is used as a building block for the development of new drug molecules. Its dibasic acid nature enables it to form salts and esters, which can be utilized in the creation of pharmaceutical formulations.
Used in Polymer and Resin Production:
2,9-dibutyldecanedioic acid is used as a monomer in the production of polymers and resins. Its incorporation into these materials can influence their properties, such as flexibility, strength, and durability, making it a useful component in the development of new materials for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 45266-20-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,5,2,6 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 45266-20:
(7*4)+(6*5)+(5*2)+(4*6)+(3*6)+(2*2)+(1*0)=114
114 % 10 = 4
So 45266-20-4 is a valid CAS Registry Number.
45266-20-4Relevant academic research and scientific papers
A cogeneration capacitor stage 2-butyl decanedioic acid and 2,9-dibutyl sebacic acid method
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Paragraph 0027; 0033; 0034, (2017/01/23)
The invention relates to a co-production method for capacitance-grade 2-butylsebacic acid and 2, 9-butylsebacic acid. The co-production method comprises the steps of carrying out nucleophilic substitution reaction on diethyl malonate and 1, 6-dibromohexane serving as raw materials in a strong alkali solution to obtain 2, 9-bis(ethoxycarbonyl)-diethyl sebacate, then, enabling 2, 9-bis(ethoxycarbonyl)-diethyl sebacate to react with n-butyl bromide in the strong alkali solution, and distilling to obtain 2-butyl-2, 9-diethoxycarbonyldiethyl sebacate and 2, 9-dibutyl-2, 9-diethoxycarbonyldiethyl sebacate; and respectively saponifying, acidifying and carrying out decarboxylic reaction to obtain 2-butylsebacic acid and 2, 9-butylsebacic acid. Due to the improvement on a technological process, a byproduct, namely 2-butyl-8-thyoxyloctanoic acid is prevented from being generated, and high-purity 2-butylsebacic acid has more excellent electrochemical properties than 2-butyloctanedioic acid sold on the market, so that the oxidation efficiency of electrolyte is increased, and the co-production method has favorable market prospects.
