26271-50-1 Usage
Description
1,3-Dichloroacetone Ethylene Ketal, with the CAS number 26271-50-1, is a compound that is utilized in the field of organic synthesis. It is characterized by its clear liquid appearance, which indicates its potential for use in various chemical reactions and processes.
Uses
Used in Organic Synthesis:
1,3-Dichloroacetone Ethylene Ketal is used as a synthetic intermediate for the production of various organic compounds. Its chemical properties, such as being a clear liquid, make it suitable for use in a wide range of chemical reactions, allowing for the creation of diverse molecules with different applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,3-Dichloroacetone Ethylene Ketal is used as a key component in the synthesis of certain drugs. Its ability to participate in various chemical reactions enables the development of new medications with potential therapeutic benefits.
Used in Chemical Research:
1,3-Dichloroacetone Ethylene Ketal is also utilized in chemical research as a tool to study the properties and behavior of different compounds. Its clear liquid form allows researchers to observe and analyze its interactions with other substances, leading to a better understanding of chemical reactions and the development of new compounds.
Used in Environmental Applications:
1,3-Dichloroacetone Ethylene Ketal can be employed in environmental applications, such as the treatment of pollutants or the development of eco-friendly materials. Its versatility in organic synthesis makes it a valuable asset in creating solutions to environmental challenges.
Check Digit Verification of cas no
The CAS Registry Mumber 26271-50-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,2,7 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 26271-50:
(7*2)+(6*6)+(5*2)+(4*7)+(3*1)+(2*5)+(1*0)=101
101 % 10 = 1
So 26271-50-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H8Cl2O2/c6-3-5(4-7)8-1-2-9-5/h1-4H2
26271-50-1Relevant articles and documents
Synthesis method of 3-oxetanone
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Paragraph 0040-0043; 0048-0051; 0056-0059, (2020/11/25)
The invention discloses a synthesis method of 3-oxetanone. Specifically, 1, 3-dichloroacetone and ethylene glycol are taken as raw materials, 3-oxetanone is synthesized at high yield through three steps of carbonyl protection reaction, ring closing reaction and deprotection reaction. The preparation method of 3-oxetanone is a synthesis method which is high in yield, low in cost, environment-friendly, easy to operate and suitable for industrialization.
Electrosynthesis of cyclopropanone adducts
Tilborg, W. J. M. van,Plomp, R.,Ruiter, R. de,Smit, C. J.
, p. 206 - 212 (2007/10/02)
Electroreduction of α, α'-dihalo ketones to cyclopropanones (isolated as the hemiacetals or hemiacylals) is accomplished with good yields only with highly alkylated α, α'-dihalo ketones.Attempts to prepare little substituted or unsubstituted cyclopropanon
